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Hirayama Disease: All You Need To Know About This Rare Neurological Disease

In Hirayama disease patients initially notice difficulty in writing, doing fine work like buttoning the shirt, mixing food and holding objects in the hands due to weakness. Here's everything you need to know about this rare condition.

Hirayama Disease: All You Need To Know About This Rare Neurological Disease

This neurological condition usually affects young males


  1. This rare disease usually affects males
  2. It can cause difficulty in performing day to day activities
  3. Surgery is usually recommended as a treatment option

Hirayama disease is a rare disease of the nervous system presenting with weakness of one or both hands. This condition was first described by Keizo Hirayama in 1959. It is also called as brachial monomelic atrophy (MMA), juvenile segmental muscular atrophy of distal upper extremity. It is more prevalent in Asia especially Japan, India, China and few south East Asian countries. In India it is commonly seen in West Bengal, Andhra Pradesh and Telangana regions. The disease is mostly seen in males in the adolescent and early adulthood age group (15-25 years).

What causes it?

The cause of this disease is not fully known. Initially it was thought to be a progressive degenerative motor neuron disease; however it may not be so. There may be genetic factors which may predispose to the disease occurrence however no specific gene has been identified with this disorder. Hirayama disease is nonfamilial in most patients.

Symptoms of Hirayama Disease

It is insidious in onset and slowly progressive. Patients initially notice difficulty in writing, doing fine work like buttoning the shirt, mixing food and holding objects in the hands due to weakness. It usually starts in one hand and then may progresses to involve the other. Later in the course of the disease the hands become progressively thin and develop a claw deformity with useless function. Worsening of weakness when exposed to cold environments is another characteristic feature of this disease. There is usually no sensory loss and no difficulty in passing urine or stools. Rarely the disease may involve the arm and shoulder muscles. Atrophy slowly progresses and plateaus typically over the course of several years. By that time the hands are completely wasted and have no functioning capacity.


Diagnosing this disease can be tricky as it masquerades as other degenerative neurological disorders for which there is no definite treatment yet. Muscle biopsy and nerve conduction studies suggest neuronal cell death without giving clue to the cause. Routine cervical spine MRI may miss the diagnosis. There may be a Loss of normal cervical lordosis (curvature) with straight or hypnotic (reverse curvature) cervical spine alignment, but this is a nonspecific finding. No compression over the cord is evident. However on performing MRI with the neck flexed (bent forward) compression of the cervical spinal cord posteriorly by the dura (a thick protective membrane which comprehensively covers the brain and spinal cord) can be patently identified. In advanced cases there may be localised atrophy of the cervical cord.

Treatment and Prognosis

Till recently this disease was looked at with despondency and nihilism, with no specific treatment. A cervical collar with watchful expectation along with physiotherapy was the treatment option available. It may provide some relief from symptoms, though not satisfactorily. In spite of this, the disease can progress relentlessly, stabilising only after significant weakness has occurred.

Over the last few decades it is becoming clear that surgical intervention may provide some hope to this otherwise hopeless condition. The surgery involves removing an offending cervical disc and fixing the adjacent portions of the cervical spine with a plate and screws. This reduces the extent of neck bending and prevents further damage to the cervical spine. This is a technically challenging surgery done under the microscope. The disc is approached via an anterior neck incision and by displacing the trachea and esophagus to one side. It takes about an hour or two depending on the complexity, to perform the surgery. The patients are discharged on the next day after surgery and are encouraged to return to normal activities in a week or so. Following surgery a cervical collar is to be worn for 3-6 weeks along with regular physiotherapy. In most patients the disease stabilizes after surgery along with many times noticeable improvement in hand bulk and strength.

Hirayama disease is an often under recognized condition, the etiology of which is unknown. It usually affects the young male population leading to incapacitating, helpless situation of hand weakness. If timely, early diagnosis is made surgical intervention can provide a ray of hope in halting the progression and to some extent reversing the weakness in these patients.

(Dr. Dhananjaya I Bhat, Senior Consultant, Neurosurgery, Aster RV Hospital)

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