Spinal Muscular Atrophies of Childhood [spinální svalové atrofie v dětství]
- Terms
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chronická infantilní forma SMA
chronická infantilní forma spinální svalové atrofie
intermediální forma SMA
intermediální forma spinální svalové atrofie
juvenilní spinální svalová atrofie
Kugelbergův-Welanderové typ SMA
morbus Werdnig-Hoffmann II
nemoc Kugelbergova-Welanderové
SMA typ II
SMA typ III.
spinální muskulární atrofie v dětství
spinální svalová atrofie I. typu
spinální svalová atrofie II. typu
spinální svalová atrofie III. typu
spinální svalová atrofie infantilního a juvenilního typu
spinální svalové atrofie v dětském věku
svalová atrofie spinální - typ II
Werdnigův-Hoffmannův syndrom
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Infantile Spinal Muscular Atrophy
Juvenile Spinal Muscular Atrophy
Kugelberg-Welander Disease
Kugelberg-Welander Syndrome
Muscular Atrophy, Infantile
Muscular Atrophy, Juvenile
Muscular Atrophy, Spinal, Infantile
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
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, Infantile
Spinal Muscular Atrophy, Juvenile
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
Werdnig-Hoffmann Disease
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)
- Annotation
- infantile, childhood or adolescent: for other, MUSCULAR ATROPHY, SPINAL is available
- v kojeneckém, dětském nebo adolescentním věku; pro ostatní je k dispozici SPINÁLNÍ SVALOVÁ ATROFIE
- DUI
- D014897 MeSH Browser
- CUI
- M0022919
- Previous indexing
- Muscular Atrophy (1966-1987); Spinal Cord Diseases (1966-1987)
- History note
- 2000(1988)
- Public note
- 2000; see WERDNIG-HOFFMAN DISEASE 1991-1999, see MUSCULAR ATROPHY, SPINAL 1988-90
Allowable subheadings
- BL
- blood 1
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 11
- CO
- complications 1
- DI
- diagnosis 18
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy 17
- EC
- economics 2
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology 2
- GE
- genetics 20
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality 1
- NU
- nursing 4
- PS
- parasitology
- PA
- pathology 5
- PP
- physiopathology 6
- PC
- prevention & control
- PX
- psychology 1
- RT
- radiotherapy
- RH
- rehabilitation 1
- SU
- surgery
- TH
- therapy 12
- UR
- urine
- VE
- veterinary
- VI
- virology
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