Search on: INFANTILE SPINAL MUSCULAR ATROPHY 
Descriptors Found: 1
Displaying: 1 .. 1  

 1 / 1 DeCS     
Descriptor English:   Spinal Muscular Atrophies of Childhood 
Descriptor Spanish:   Atrofias Musculares Espinales de la Infancia 
Descriptor Portuguese:   Atrofias Musculares Espinais da Infância 
Synonyms English:   HMN (Hereditary Motor Neuropathy) Proximal Type I
Kugelberg-Welander Syndrome
Muscular Atrophy, Infantile
Muscular Atrophy, Juvenile
Muscular Atrophy, Spinal, Infantile Chronic Form
Muscular Atrophy, Spinal, Intermediate Type
Muscular Atrophy, Spinal, Type I
Muscular Atrophy, Spinal, Type II
Muscular Atrophy, Spinal, Type III
Proximal Hereditary Motor Neuropathy Type I
SMA, Infantile Acute Form
Spinal Muscular Atrophy 1
Spinal Muscular Atrophy Type 2
Spinal Muscular Atrophy Type I
Spinal Muscular Atrophy Type II
Spinal Muscular Atrophy Type III
Spinal Muscular Atrophy, Mild Childhood and Adolescent Form
Spinal Muscular Atrophy, Type 3
Spinal Muscular Atrophy, Type I
Spinal Muscular Atrophy, Type II
Spinal Muscular Atrophy, Type III
Type I Spinal Muscular Atrophy
Type II Spinal Muscular Atrophy
Type III Spinal Muscular Atrophy
Werdnig Hoffman Disease
Infantile Muscular Atrophy
Juvenile Muscular Atrophy
Kugelberg Welander Disease
Kugelberg Welander Syndrome
Werdnig Hoffmann Disease
Infantile Spinal Muscular Atrophy
Muscular Atrophy, Spinal, Infantile
Spinal Muscular Atrophy, Infantile
Werdnig-Hoffmann Disease
Juvenile Spinal Muscular Atrophy
Kugelberg-Welander Disease
Spinal Muscular Atrophy, Juvenile  
Tree Number:   C10.228.854.468.800
C10.574.500.812
C10.574.562.500.750
C10.668.467.500.750
C16.320.400.765
Definition English:   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) 
Indexing Annotation English:   infantile, childhood or adolescent: for other, MUSCULAR ATROPHY, SPINAL is available
History Note English:   2000(1988) 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DG diagnostic imaging DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   24374 
Unique Identifier:   D014897 

Occurrence in VHL: 		 

Similar:
  
DeCS CID-10 LILACS