Muscular Dystrophy Association Clinic
The JFK Johnson Rehabilitation Institute's Muscular Dystrophy Association (MDA) Clinic provides a multidisciplinary approach to the diagnosis and treatment of over 40 muscular dystrophies. Adult and pediatric clinics are held once a month throughout the year. Services consist of examination, testing and counseling performed by a physiatrist, physical, occupational and speech therapist. A social worker and registered nurse also assist in assessing the patient's/family's needs. After establishing the diagnosis and treatment plan, the patient is monitored two to three times a year through follow-up clinic visits.
The clinic, partially supported by the Muscular Dystrophy Association through a grant, is one of 230 hospital-based clinics affiliated with the MDA. If you suspect that you or your child may have the diagnosis of muscular dystrophy, you may call for a clinic appointment. Appointments for the adult clinic can be made by calling (732) 321-7733 and the pediatric clinic can be reached at (732) 548-7610.
Diseases treated through the MDA clinic include:
Muscular dystrophies
- Myotonic Dystrophies
- Duchenne's
- Becker's
- Limb-Girdle
- Facioscapularhumeral
- Congenital
- Distal
- Emery-Dreifus
Motor neuron diseases
- Amyotrophic lateral sclerosis(ALS)
- Infantile progressive spinal muscular atrophy
(Type 1 Werdnig Hoffman disease)
- Intermediate Spinal Muscular Atrophy (Type 2)
- Adult Spinal Muscular Atrophy (Aran-Duchenne type)
Inflammatory myopathies
- Polymyosititis
- Dermatatomyositis
Diseases of the Neuromuscular junction
- Myasthenia Gravis
- Eaton-Lambert (myasthenic) syndrome
Diseases of the Peripheral Nerve
- Peroneal muscular atrophy (Charcot Marie Tooth Disease)
- Frederick's Ataxia
- Dejerine-Sottas disease
- Metabolic Diseases of the Muscle
- Phosphorylase deficiency(McArdles disease)
- Acid Maltase Deficiency (Pompe's disease)
- Phosphofructokinase deficiency(Tauri's disease)
- Debrancher Enzyme Deficiency (Cori or Forbes' disease)
- Mitochrondrial myopathy
- Carnitine deficiency
- Phosphoglycerate kinase deficiency
- Phosphoglycerate mutase deficiency
- Lactate dehydrogenase deficiency
- Myoadenylate deaminase deficiency
Myopathies due to Endocrine Abnormalities
- Hyperthyroid myopathy
- Hypothyroid myopathy
Other Myopathies
- Myotonia congenita
- paramyotonia congenita
- Central core disease
- Nemaline myopathy
- Myotubular myopathy
- Periodic paralysis
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