Spinal Muscular Atrophies of Childhood
A group of recessive inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3)
推出的年份: 2000(1988)
树号: C10.228.854.468.800, C10.574.500.812, C10.574.562.500.750, C10.668.467.500.750, C16.320.400.765
MeSH 单一 ID: D014897
进入的组:
Muscular Atrophy, Spinal, Type II
Spinal Muscular Atrophy Type 2
Type II Spinal Muscular Atrophy
Spinal Muscular Atrophy Type II
Spinal Muscular Atrophy, Type II
HMN (Hereditary Motor Neuropathy) Proximal Type I
Spinal Muscular Atrophy, Infantile
Muscular Atrophy, Spinal, Infantile
Werdnig-Hoffmann Disease
Werdnig Hoffmann Disease
Muscular Atrophy, Spinal, Type I
Spinal Muscular Atrophy Type I
SMA, Infantile Acute Form
Type I Spinal Muscular Atrophy
Proximal Hereditary Motor Neuropathy Type I
Werdnig Hoffman Disease
Muscular Atrophy, Infantile
Infantile Muscular Atrophy
Spinal Muscular Atrophy 1
Infantile Spinal Muscular Atrophy
Spinal Muscular Atrophy, Type I
Juvenile Spinal Muscular Atrophy
Spinal Muscular Atrophy Type III
Spinal Muscular Atrophy, Type III
Type III Spinal Muscular Atrophy
Muscular Atrophy, Juvenile
Juvenile Muscular Atrophy
Kugelberg-Welander Disease
Kugelberg Welander Disease
Spinal Muscular Atrophy, Type 3
Kugelberg-Welander Syndrome
Kugelberg Welander Syndrome
Spinal Muscular Atrophy, Mild Childhood and Adolescent Form
Spinal Muscular Atrophy, Juvenile
Muscular Atrophy, Spinal, Type III
Muscular Atrophy, Spinal, Infantile Chronic Form
Muscular Atrophy, Spinal, Intermediate Type
早前的内容:
Muscular Atrophy (1966-1987)
Spinal Cord Diseases (1966-1987)
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