Best Hemifacial Spasm Treatment in India

Best Hemifacial Spasm Treatment in India

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Dedicated to the Focus and International Excellence in MVD Surgery for Hemifacial spasms and Trigeminal Neuralgia, by Dr Jaydev Panchawagh and Team.

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14/05/2026

“Every Case Is a Universe Unto Itself”
A conversation with Dr Jaydev Panchwagh on MVD surgery, neurovascular conflict, and a 22-year journey from Pune to the world
Synapse Brain and Spine Institute, Pune, India • Supported by Synapse Brain and Spine Foundation & Neurochirurgische Hilfe Indien, Aalen, Germany

Dr Jaydev Panchwagh is a neurosurgeon based in Pune, India, who has spent over two decades building one of the world’s largest single-surgeon experiences in Microvascular Decompression (MVD) surgery — a delicate procedure performed at the base of the skull to treat neurovascular conflict syndromes including trigeminal neuralgia, hemifacial spasm, and glossopharyngeal neuralgia. His work is supported by the Synapse Brain and Spine Foundation in Pune and by Neurochirurgische Hilfe Indien, an Indo-German neurosurgery support foundation based in Aalen, in southern Germany. We spoke with him after a day in the operating theatre.

Dr Panchwagh, you performed two MVD surgeries today. Can you describe what a typical day at your centre looks like?
On any given day, we may have two MVD surgeries, sometimes three. At other times we are operating on brain tumours or managing various cases across brain and spine. But MVD surgery has been the core focus here for the last 22 years. We established this centre in Pune in 2004 specifically as a focused centre for neurovascular conflict syndromes, and that philosophy has not changed.
What exactly is a neurovascular conflict, and why does it matter?
A neurovascular conflict — also called neurovascular compression (NVC) — occurs when a blood vessel, usually an artery, makes abnormal contact with a cranial nerve at its root entry zone near the brainstem. Over time, this pulsatile compression irritates the nerve and causes symptoms that can be profoundly disabling. In trigeminal neuralgia, patients experience electric-shock-like facial pain, often triggered by eating, speaking, or even a breeze. In hemifacial spasm, there is involuntary twitching of one side of the face. In glossopharyngeal neuralgia, the pain affects the throat and ear. These are not rare conditions — they are simply under-diagnosed, and many patients suffer for years before reaching the right specialist.
MVD surgery relieves the compression by placing a small Teflon cushion between the offending vessel and the nerve. When done well, it offers durable, long-term relief without damaging the nerve — which makes it superior to ablative procedures for the right patient.
You have now crossed 2,700 MVD surgeries personally. How significant is that number?
Going by the statistics from about a month ago, we have crossed 2,700 total MVD surgeries performed by me personally, with a fairly constant team. Today’s two cases were, in fact, the 751st and 752nd in just the last five years alone. I believe this is certainly one of the largest single-surgeon, single-team experiences in MVD surgery globally.
But the number is not mentioned for any record or vanity. The importance is entirely scientific. We maintain extremely meticulous records — not just with me, but in the operation theatre register and the hospital registry. Every year we audit this data and report it at an international conference. We have been doing so consistently for the last four years. Our research papers are ongoing, and a book is in preparation, with some parts already in print.
How does surgical volume actually translate into better outcomes for patients?
It is a very important question, and the answer is more nuanced than people expect. In MVD surgery, there are an enormous number of variables in individual anatomy and neuroanatomic detail. Take trigeminal neuralgia alone — there are about 14 distinct anatomical variables. If each variable has roughly six possible presentations, the net number of anatomical variations crosses 700 million. And I am not even counting the medical variables specific to an individual patient, which have a direct bearing on how the surgery must be conducted.
So what does experience do? With time, you start identifying gross patterns early. You know where to look based on what you have seen before. You develop a feel for how much a cranial nerve can be safely handled, how far a blood vessel can be mobilised, where to stop, and where to be especially careful. There is substantial literature confirming that experience — applied consciously and conscientiously — has an enormous impact on outcomes and on reducing complication rates. We have audited our own data and seen this reflected year on year.
The statement about numbers, therefore, is entirely about the patient’s wellbeing. That is its only relevance.
Your patients come from far beyond Pune. Can you describe the reach of the programme?
We have operated on patients with neurovascular conflict syndromes from almost every state in India. And beyond India, we have treated patients from 15 countries across the world — across Asia, the Middle East, Africa, Europe, and beyond. This international patient population has added a significant dimension to our experience: we are now operating across different ethnicities and different genetic variables, which introduces its own set of anatomical and physiological nuances. Cranial base anatomy, vascular geometry, and nerve characteristics do show population-level differences, and having this breadth of exposure has deepened our understanding considerably.
This is also why discoverability matters. A patient in Nigeria or Malaysia or the United Kingdom suffering from trigeminal neuralgia deserves to know that effective surgical treatment exists and that experienced centres are available. Part of our responsibility is to make that information accessible.
You mentioned institutional support. Who are your key partners?
The programme is supported by the Synapse Brain and Spine Foundation here in Pune, which facilitates the research, documentation, and patient support infrastructure. We are also supported by Neurochirurgische Hilfe Indien — which translates as Neurosurgery Help India — an Indo-German foundation based in Aalen in southern Germany. Their support has been meaningful both in terms of international academic exchange and in enabling access to care for patients who might otherwise not be able to reach us.
You have also developed a large patient support network. How did that come about?
Patients with trigeminal neuralgia and hemifacial spasm often endure years of misdiagnosis and ineffective treatment before finding their way to the right intervention. The suffering is not only physical — it is deeply isolating. Building large patient support groups was a natural extension of the clinical work. These communities serve a practical purpose: patients share experiences, guide one another to the right resources, and provide a peer understanding that no clinician can fully substitute. They have become a significant part of the programme.
You have also pursued a more unusual line of work — the neuroaesthetics project. What is that?
Over the years, I have drawn the neuroanatomy of neurovascular conflicts by hand — detailed illustrations of what we encounter at surgery. This has created a large library of anatomical drawings used for teaching and research. Over time, around a hundred of these drawings evolved into something more intentional — they became aesthetic paintings, each one rooted in surgical anatomy but composed as a work of art.
From this, we developed what we call the neuroaesthetics project, which sits at the intersection of neuroscience and visual art. In 2023, a selection of these paintings was displayed at an international conference, and the reception was very encouraging — they generated genuine interest and applause from the neurosurgical community. The aim is to use art as a medium for communicating complex neuroanatomy in a way that is accessible, memorable, and even beautiful. Science does not have to be dry.
What are the rarer indications for MVD surgery that are not widely known?
Beyond trigeminal neuralgia and hemifacial spasm, MVD surgery can address glossopharyngeal neuralgia — severe pain in the throat and ear. It has also been used for very resistant cases of tinnitus, and very rarely for severe vertigo that can be clearly attributed to neurovascular compression both clinically and radiologically. Then there are rare syndromes such as vagoglossopharyngeal syndrome, in which glossopharyngeal neuralgia is accompanied by syncope — sudden, brief loss of consciousness — due to involvement of the vagus nerve. These are uncommon presentations, but they are important to recognise because they are surgically treatable.
A final thought for patients around the world who may be reading this?
If you or someone you know has been living with facial pain, hemifacial spasm, or any of the conditions we have discussed — and has not found relief through medication — please know that effective surgical options exist. Microvascular decompression, when performed by an experienced team, offers durable and meaningful relief without destroying the nerve. You do not have to keep suffering.
More broadly, I hope that the philosophy behind MVD surgery — surgical intervention aimed at restoring function rather than simply ablating it — continues to expand across neurology. There are many conditions yet to benefit from this thinking. That is the work ahead.
**************************
Ref;

Dr Jaydev Panchwagh • Synapse Brain and Spine Institute, Pune, India • Neurovascular Conflict • MVD Surgery • Trigeminal Neuralgia • Hemifacial Spasm • Glossopharyngeal Neuralgia • Microvascular Decompression • Neurochirurgische Hilfe Indien, Aalen, Germany
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10/05/2026

Simple and precise explanation of why Hemifacial spasms need to be treated by brain surgery for permanent cure.
Please watch and forward.
It is a part of Public education series in behalf of the Synapse Brain and Spine Foundation.

Hemifacial Spasm Explained By India's Top Brain Surgeon 02/04/2026

Do you( or someone you know) have persistent eye twitches that has progressed to half-face twitching? Do the spasms worsen with anxiety or social interactions? This could be indicative of Hemifacial Spasm!
A cure is possible with the right neurosurgeon who does MVD surgery several times a week.

Learn more:

Hemifacial Spasm Explained By India's Top Brain Surgeon Hemifacial spasm, as explained by India's top brain surgeon, is a nerve disorder caused by an abnormal contact between tha Facial Nerve and one or more blood...

Hemifacial Spasm Explained By India's Top Brain Surgeon 01/04/2026

Q1: What exactly is Hemifacial Spasm, and how does it start?
A: Hemifacial Spasm (HFS) is a neurological disorder where one side of the face experiences involuntary muscle contractions. It typically starts subtly, often with twitching in the lower eyelid, which many people mistake for fatigue. Gradually, it spreads down the face to the cheek and mouth. [03:10]

Q2: What is the primary cause of these involuntary spasms?
A: The most common cause is a "Neurovascular Conflict." This occurs when a blood vessel (artery or vein) is in direct contact with the facial nerve where it exits the brainstem. The constant pulsation of the blood vessel "hammers" the nerve, wearing down its protective insulation (myelin) and causing the nerve to misfire. [04:29]

Q3: How is Hemifacial Spasm different from Bell's Palsy?
A: They are clinical opposites. In Bell's Palsy, the facial nerve is damaged such that the muscles become paralyzed and cannot move. In Hemifacial Spasm, the nerve is hyper-excited, causing the muscles to move too much and without the patient's control. [07:17]

Q4: Why is a standard MRI often insufficient for diagnosis?
A: A standard brain MRI might not show the fine detail of the nerve and blood vessel intersection. Diagnosis requires a high-quality 3-Tesla MRI with specific sequences (like FIESTA or CISS) interpreted by a radiologist who knows what to look for at the "Root Entry Zone." [09:04]

Q5: Is Botox a recommended long-term solution for HFS?
A: No. While Botox is a common first-line treatment, it is only a temporary mask. It works by paralyzing the muscles, but the underlying nerve compression continues. Over time, the body builds resistance, the effects wear off faster, and it can cause permanent facial weakness. [10:43]

Q6: What is Microvascular Decompression (MVD) surgery?
A: MVD is the only curative surgery for HFS. A neurosurgeon makes a small incision behind the ear, identifies the conflicting blood vessel, and moves it away from the nerve. A small piece of Teflon is then placed between them to act as a permanent cushion. [13:17]

Q7: What is the success rate of MVD surgery according to Dr. Panchwagh?
A: With an experienced surgical team, the permanent cure rate is approximately 99%. Dr. Panchwagh's center has performed over 770 of these specific procedures, making it one of the most experienced centers globally. [16:51]

Q8: What are the social and psychological consequences of HFS?
A: HFS is often "socially disabling." Patients face extreme anxiety in public settings because their face twitches uncontrollably. Dr. Panchwagh shares stories of patients being ridiculed, losing jobs, or facing marital strain because others misinterpret the spasms as intentional winking or strange behavior. [22:40]

Prof Dr Jaydev Panchwagh
MS, MCh Neurosurgery
Brain and Spine surgeon
*Chairman- Synapse Brain and Spine Foundation
*Founder Member Neurochirurgische Hilfe Indien
(Indo German Neurosurgery Foundation)
*You Tube Channel - "Dr Jaydev Panchawagh"

www.neurosurgerypune.com
www.drjaydev.com

Facebook- 'Dr Jaydev Panchwagh-Neurosurgeon'

You tube Channel- 'Dr Jaydev Panchwagh'

https://youtu.be/1ZZgk_qAp4M?si=GLuvc_UE_VSS_o9g

Hemifacial Spasm Explained By India's Top Brain Surgeon Hemifacial spasm, as explained by India's top brain surgeon, is a nerve disorder caused by an abnormal contact between tha Facial Nerve and one or more blood...

28/03/2026

𝐀 𝐂𝐫𝐨𝐨𝐤𝐞𝐝 𝐒𝐦𝐢𝐥𝐞
A Neurosurgeon's Insight into Spasms of the face.
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In the world of neurological disorders there is a particular Neurological condition that we have been treating for more than two decades. With a constant focus on the treatment outcomes, research, public education and surgical excellence.
This neurological problem does not kill. It does not blind. It leaves no visible scar. And yet, in the severe devastation it delivers to ordinary life, it ranks among the cruelest disorders I have encountered in a career spent operating inside the human nervous system.

It is called Hemifacial Spasm —or HFS, in the shorthand of neurology. In Marathi, lacking a precise equivalent, I once I had named it myself in an article.
"The disease of the winking eye."
Or simply, "Winking disorder"
The name stuck and it fits, with uncomfortable accuracy.

Over the past twenty years, practising out of the city of Pune which is considered the hub of education and culture in India, we dedicated ourselves to this particular corner of neurosurgery, called as Microvascular Decompression.
In the course of this project, I have met hundreds of patients carrying this condition. I have watched it shrink lives. I have watched it end marriages, cost jobs, and confine spirited human beings to the narrow shelter of their own homes. And I have, thankfully, watched surgery set most of them free.

This is what I want to write about. Not the disease alone, but the disturbing stories it produces. The misunderstanding that surrounds it.
And most importantly, the treatment that exists but remains, bewilderingly, unknown to the most who actually need it.

So what Exactly Happens in HFS?
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Picture the face of someone you know. Now imagine, that, without warning or invitation, one side of that face begins to move on its own...in twitches, in spasms

It begins small. A flutter near the eye. A twitch of the eyelid — the kind every tired person has felt at the end of a long day. Easy to dismiss. Easy to wait out. But in hemifacial spasm, the waiting changes nothing. The flutter does not subside. It returns. It returns more often. It becomes a wink.

Over months and years, the spasm migrates southward along the face. The cheek joins the eye. Then the corner of the mouth. One entire side of the face begins to contract, repeatedly and without consent and without notice.
Repeated, uncontrollable, involuntary, sudden facial twitches or spasms in rapid succession. Particularly in the most important social settings — at the bank counter, the classroom, the reception desk, the dinner table — the affected person appears to be winking deliberately. Suggestively. Provocatively.

Actually, they are doing none of these things. They have no more control over that wink or one sided facial contractions than over the beating of their heart.

Among the many patients I have seen, some stories refuse to leave me.

Sandeep was in his mid-thirties, and he came to our clinic with his wife Swati. He held his right hand cupped against the right side of his face — a gesture I have seen so many times now that I recognise it before a patient even sits down. It is the posture of someone trying to hide themselves from the world.

Swati told me what had happened the previous week. Sandeep had been standing at a bus stop in Mumbai, reading a magazine while he waited. Occasionally he looked up to check for the bus. The spasms on his face were doing what they always did — moving involuntarily, the right eye blinking open and shut in rapid, rhythmic contractions.

The woman standing to his right turned on him suddenly. She was furious. She said: 'Aren't you ashamed? Winking like that? Do it again and I will call the police.'

Before he could explain, two bystanders had struck him.

This happened. It is not embellished. I write it as it was told to me, by the man who lived it.

From Chennai: a young woman who worked at the reception desk of a prominent company. She greeted visitors. She answered questions. She smiled. At thirty-two, the spasms arrived on the right side of her face. She could no longer look people in the eye without the eye winking back at them, beyond her command. She lost the job she had built her career around.

From Jharkhand: a young man whose marriage proposals kept dissolving before they could take root. From Mumbai: a man whose marriage ended. From Kerala: a sixty-five-year-old who had not slept soundly in years because the spasms did not pause for the night. From Africa: a young man who told me, with a quiet sadness I still remember, that no woman on any bus would sit across from him.

And from across India, and indeed across the world...
I hear this sentence at our MVD surgery centre... after successful MVD surgery has finally brought relief:
Patients lamenting in frustration
'If only I had known this could be cured. If only someone had told me. The years I lost !!!!!'

To understand why HFS happens requires a small journey into the architecture of the brain's base — that quiet, crowded neighbourhood at the skull's floor where cranial nerves emerge before fanning out into the face and beyond.

The facial nerve — the seventh cranial nerve — is responsible for the movement of every muscle of expression on the face. It is the nerve that allows you to smile, to frown, to blink, to squint. It arises from the brainstem and immediately travels through a narrow corridor of bone and fluid.

This nerve has a peculiarity. Near its origin, at the point where it exits the brainstem, it has a brief stretch where its protective myelin sheath changes.its character from centralyelin to peripheral myelin.
Usually this transition is smooth....like perfect stitching of a shirt sleeve.
But occasionally, in defective pieces you do get defective shirts in which the stitching is weak and incomplete.
Similarly some facial nerve myelin sheath is not "Stiched" properly at this delicate zone called as the "Root Exit Zone". There are potential gaps.
Imagine an electrical cable with wires tightly packed inside. And then imagine that the insulation rubber coatings of the wire are freyed and thinned out at the place where the wire is entering into the electrical appliance.
Any further pressure there will cause complete loss of insulation and a short circuit.
Something like this happens in some facial nerves.
This is not very uncommon defect.. Under ordinary circumstances it causes no difficulty at all.

But suppose a blood vessel — one of the small arteries that loop and wander near the brainstem — comes to rest against this vulnerable segment of the nerve. And suppose that vessel pulsates, as all arteries do, with each heartbeat.

With each pulse, the artery taps the nerve. Tap, tap, tap. Thousands of times a day. Hundreds of thousands of times a year.
This is called as the "Neurovascular conflict"
in neurosurgical language.

At first, this produces little problems. The nerve is resilient. But over time, the relentless percussion begins to erode the myelin — the nerve's electrical insulation. Again think of the wire, whose rubber coating has been worn down by repetitive friction. When insulation fails, signals begin to short-circuit. Impulses that should have stayed inside the nerve's fibres begin to spill across to neighbouring fibres. The facial muscles start receiving signals they were never sent. They contract. They spasm.

The body, meanwhile, does not help matters. As we age, our blood vessels lengthen and begin to coil — a process that has the technical name dolichоectasia, but which is simply the slow arterial elongation that comes with the passage of years. As the artery grows longer and more tortuous, it presses harder against the nerve. The symptoms deepen. The spasms become more frequent, more forceful, more socially catastrophic.

Some patients also report a faint ringing in the ear on the affected side. Others notice a temporary reduction in hearing when the spasms are at their worst. These are not coincidences. The cochleovestibular nerve, responsible for hearing and balance, runs close to the facial nerve. When the artery's pressure is great enough, it affects both.
Also, the facial nerve supplies the shortest muscle in human body which is inside of the middle ear. If the facial impulses short circuit to this muscle during spasms, it contracts. This contraction dampens hearing.

MVD .. Surgery That Cures
***************************

There is one and only one treatment in the world that addresses the cause of hemifacial spasm rather than its symptoms. It is called Microvascular Decompression, or MVD.

The principle is elegant in its logic. If the problem is a pulsating artery pressing against a nerve, the solution is to separate them. Through a small opening behind the ear, a neurosurgeon reaches the base of the skull, identifies the offending vessel, and places a small cushion — a pad of Teflon — between artery and nerve. The mechanical irritation ends. In the months that follow, the damaged myelin regenerates. The short-circuits cease. The spasms stop.

The surgery is technically demanding. The anatomy at the base of the skull leaves no margin for imprecision. But in the hands of an experienced, dedicated team performing these procedures regularly and in volume, the outcomes are remarkable. In our centre in Pune, established in 2004 with a specific focus on trigeminal neuralgia and hemifacial spasm, we have performed more than seven hundred such operations. The results have been presented at national and international conferences from 2014 through 2025.

"We are what we repeatedly do. Excellence, then, is not an act, but a habit." — Aristotle

That line by Aristotle is not merely decorative. It is the operating philosophy of a surgical team. The surgeon who performs MVD twice a year is not the same surgeon as the one who performs it forty times a year. Volume builds precision. Repetition sharpens judgement. Habit, in surgery as in art, is where excellence actually lives.

On Botulinum Toxin: An Honest Reckoning
*********************

Patients often ask me about Botox — the injection of botulinum toxin into the facial muscles to temporarily paralyse them, silencing the spasms for a few months at a time. Do I oppose it? No. Every person has the right to choose their own treatment.

But I owe my patients clarity, and clarity requires honesty.

Botulinum toxin — produced by the bacterium Clostridium botulinum — is a genuine and powerful pharmacological tool. Used appropriately, in conditions where no curative treatment exists, it offers meaningful relief. For hemifacial spasm specifically, it is frequently used to quiet the muscles by inducing a temporary and controlled paralysis.

The word temporary is the one that matters.

The effect wears off. The injections must be repeated, every few months, indefinitely. After each injection, the face can feel heavy and stiff. And underneath that artificial stillness, the nerve-compression that caused everything continues unchanged, unaddressed, quietly worsening. The artery still presses. The myelin still degrades. The injury to the nerve deepens, month by month, year by year.

The longer a patient defers surgery in favour of repeated botulinum injections, the more severe the nerve damage becomes — and the less certain the eventual surgical outcome. This is not a theoretical concern. It is what the anatomy demands.

I do not say this to frighten anyone away from botulinum toxin. I say it because this information is rarely provided when the injections are recommended. Patients are not told. They should be.

The Dimension That Medicine Forgets
***********************
The medical literature on hemifacial spasm is precise about the nerve and the artery. It is less articulate about what the condition does to a person's interior life.

Human faces are the medium through which we communicate almost everything that words do not carry. Trust. Interest. Warmth. Safety. When a face begins to move in ways its owner cannot govern, the very instrument of social connection becomes a source of alarm and misunderstanding. The person living inside that face retreats.

They stop attending office meetings. They decline invitations to weddings and celebrations. They avoid any situation involving strangers. They reroute their daily lives to avoid being seen.

The occupational consequences are particularly severe for those whose work requires constant human interaction — teachers, police officers, nurses, doctors, sales staff, receptionists, actors, performers. The list, as I have written in Marathi and repeat here, is essentially endless. For these individuals, the spasm is not merely a medical inconvenience. It is a professional extinction.

The psychological toll compounds over years. Patients describe shame. They describe the exhaustion of constant explanation and the futility of that explanation when no explanation is accepted. They describe the specific grief of watching their own face betray them, in public, without warning, without mercy.

What Every Patient Deserves to Know
***********************
The single thing I most want the reader to take from this piece is simple: hemifacial spasm can be cured.

Not managed. Not suppressed temporarily. CURED !!
The word means what it says — the abnormal pulsation is removed, the nerve recovers, the spasms cease, and the patient reclaims their face and, along with it, their life.

This truth is not being communicated adequately. Patients spend years — sometimes decades — cycling through botulinum injections, reassurances that nothing serious is wrong, and the private indignity of being mistaken for someone who is deliberately winking at strangers and also suffering from the physical problems due to the spasms.
The information gap is itself a kind of harm.

Our centre established its counselling programme for exactly this reason. Before any surgical decision is made, we spend time ensuring that a patient genuinely understands what is happening inside their brainstem, what options exist, what surgery involves, and what the realistic expectations of recovery are. We are not unmindfully insistent for surgery though we have very high conviction based on our 20 years of experience.
We have experience of 775 stories of HFS who underwent MVD at our hands.
We have had our share of failures, which is 1%.
We have had our share of complications, which have reduced over the period of time, with increasing experience of the team.
We do not shy away from discussing rare possible risks with the patients before surgery.
But we think and insist that the problems, the failures, the risks, which are statistically miniscule need to be discussed in the right perspective.
We know that a risk, which is statistically 0.2 percent, is 100 percent for the patient in whom it occurs.
It is true about all the risks involved we take while leading normal life. It is true about all the stats.
But the risks have to be compared with the risk, no, actually the 'certainty' of the life becoming unbearingly and progressively crooked due to spasms. We need to remember that HFS is, by and large, a 'progressive' disorder. (Even though in the initial phase there could be periods of spasm holidays)

We are advocates for informed choice.

Our aim is not to fanatically convince anyone to undergo MVD.
But no one should be deprived of the knowledge that surgery exists, that it works wonderfully especially if performed by experienced and well equipped team and that for most patients with this condition, it offers the only path to being permanently well.

Modern neurosurgery holds this answer. Our obligation — at the MVD surgery centre, — is to make sure the people who need this answer can actually find it.

Dr Jaydev Panchawagh
— — —
The author is a neurosurgeon based in Pune, with a specialised focus on MVD surgeries for trigeminal neuralgia and hemifacial spasm
since 2004.

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