Sciensano manages the content of the Belgian neuromuscular diseases registry (BNMDR) since 2008. The registry is essential for the development of new treatments for neuromuscular diseases.

A neuromuscular disease affects the peripheral nerves (i.e., all nerves in the body, except for those of the brain and spinal cord), the muscles, or the connections between the nerves and muscles. These diseases are rare, often severe, and sometimes fatal. They occur in both children and adults. People with a neuromuscular disease often lose muscle strength either in a specific part of their body or in their entire body, causing disabilities and suffering on a daily basis.
Please note, they are not diseases such as Parkinson’s disease or multiple sclerosis, which affect the central nervous system (brain and/or spinal cord). Neuromuscular diseases affect the peripheral nervous system (i.e., the nerves and muscles of your arms, legs, trunk, … which allow movement and touch).
Currently, there are few treatments for neuromuscular diseases. However, thanks to ongoing scientific research, new drugs are discovered each year.
In total, according to the classification used, between 62 and 371 different neuromuscular diseases exist. Some of them have a genetic origin. Here is an overview:
Congenital muscular dystrophy (link is external)
Duchenne muscular Ddstrophy (link is external)
Becker muscular dystrophy (link is external)
Dystrophinopathy (link is external)
Facioscapulohumeral dystrophy (link is external)
Limb-girdle muscular dystrophy (link is external)
Emery-Dreifuss muscular dystrophy (link is external)
Distal myopathy (link is external)
Oculopharyngeal muscular dystrophy (link is external)
Thomsen disease (link is external)
Becker disease (link is external)
Central core disease (link is external)
Multiminicore disease (link is external)
Nemaline myopathy (link is external)
X-linked myotubular myopathy (link is external)
Centronuclear myopathy (link is external)
Congenital fibre-type disproportion myopathy (link is external)
Musclar glycogenosis (link is external)
Disorders of fatty acid oxidation and ketone body metabolism (link is external)
Mitochondrial myopathy (link is external)
Polymyositis (link is external)
Amyotrophic lateral sclerosis (link is external)
Progressive muscular atrophy (link is external)
Postpolio syndrome (link is external)
Primary lateral sclerosis (link is external)
Spinal muscular atrophy type 1 (Werdnig-Hoffmann disease) (link is external)
Spinal muscular atrophy type 2 (intermediate spinal muscular atrophy) (link is external)
Spinal muscular atrophy type 3 (Kugelberg-Welander disease) (link is external)
Spinal muscular atrophy type 4 (adult form) (link is external)
X-linked bulbospinal muscular atrophy (Kennedy disease) (link is external)
Hereditary motor and sensory neuropathy (link is external)
Hereditary neuropathy with liability to pressure palsies (link is external)
Hereditary sensory and autonomic neuropathy (link is external)
Guillain-Barré syndrome (link is external)
Chronic inflammatory demyelinating polyneuropathy (link is external)
Multifocal motor neuropathy (link is external)
Peripheral neuropathy associated with monoclonal gammopathy (link is external)
Polyneuropathy-endocrinopathy-plasma cell dyscrasia syndrome (POEMS syndrome) (link is external)