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Results 1 - 10 of 17 for Spinal muscular atrophy type 4
  1. ... have three or four copies, and those with type IV have four or more copies. Other factors, many unknown, also contribute to the variable severity of spinal muscular atrophy. SMN1 SMN2 Spinal muscular atrophy is inherited in ...
  2. ... 5 Distal hereditary motor neuronopathy, type V Distal spinal muscular atrophy, type V DSMAV HMN V Spinal muscular atrophy, distal ... Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V. Am J Hum Genet. 2003 May;72( ...
  3. ... characterizations of rare UBA1 variants in X-linked Spinal Muscular Atrophy. F1000Res. 2017 Sep 4;6:1636. doi: 10.12688/f1000research.11878.1. ...
  4. Distal hereditary motor neuropathy, type II is a progressive disorder that affects nerve cells in the spinal cord. It results in muscle weakness and affects ...
  5. ... paraplegia). The spasticity and paraplegia result from degeneration (atrophy) of motor neurons, which are specialized nerve cells in the brain and spinal cord that control muscle movement. Hereditary spastic paraplegias are divided into two types: pure and complicated. The pure types involve only ...
  6. ... movement. These nerve cells are found in the spinal cord and the brain. In ALS, motor neurons die (atrophy) over time, leading to muscle weakness, a loss of muscle mass, and an inability to control movement.There are many different types of ALS; these types are distinguished by their ...
  7. ... disturbances in the nerves connecting the brain and spinal cord to muscles ... atrophy, a particular type of muscle fibers (type II fibers) break down ...
  8. ... hypoplasia are designated as type 1 (PCH1) and type 2 (PCH2). In addition ... spinal muscular atrophy. Individuals with PCH1 also have very weak muscle ...
  9. ... complex hereditary spastic paraplegia because it involves all four limbs as well ... the brain and spinal cord to muscles and sensory cells that detect ...
  10. ... DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), ...
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