WERDNIG HOFFMAN DISEASE
\wˈɜːdnɪɡ hˈɒfmən dɪzˈiːz], \wˈɜːdnɪɡ hˈɒfmən dɪzˈiːz], \w_ˈɜː_d_n_ɪ_ɡ h_ˈɒ_f_m_ə_n d_ɪ_z_ˈiː_z]\
Definitions of WERDNIG HOFFMAN DISEASE
Sort: Oldest first
-
autosomal recessive disease in which the degeneration of spinal nerve cells and brain nerve cells leads to atrophy of skeletal muscles and flaccid paralysis; death usually occurs in early childhood
By Princeton University
-
autosomal recessive disease in which the degeneration of spinal nerve cells and brain nerve cells leads to atrophy of skeletal muscles and flaccid paralysis; death usually occurs in early childhood
By DataStellar Co., Ltd
-
A group of recessively 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)
By DataStellar Co., Ltd
Word of the day
basidiomycota
- comprises fungi bearing the spores on basidium: Gasteromycetes (puffballs); Tiliomycetes (comprising orders Ustilaginales (smuts) and Uredinales (rusts)); Hymenomycetes (mushrooms; toadstools; agarics; bracket fungi); in some classification systems considered a division of kingdom comprises fungi bearing spores on a basidium; includes Gasteromycetes (puffballs) Tiliomycetes comprising the orders Ustilaginales (smuts) and Uredinales (rusts) Hymenomycetes (mushrooms, toadstools, agarics bracket fungi).
Nearby Words
- wepon
- weppen's test
- wept
- wera
- werche
- Werdnig Hoffman Disease
- werdnig hoffman diseases
- werdnig hoffmann disease
- werdnig-hoffmann type
- were
- weregild