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Werd·nig-Hoff·mann disease

n :  atrophy of muscles that is caused by degeneration of the ventral horn cells of the spinal cord, is inherited as an autosomal recessive trait, becomes symptomatic during early infancy, is characterized by hypotonia and flaccid paralysis, and is often fatal during childhood - called also Werdnig-Hoffmann syndrome  - compare KUGELBERG-WELANDER DISEASE 
Werdnig, Guido (1844-1919),
Austrian neurologist, and Hoffmann, Johann (1857-1919), German neurologist. Independently of each other, Werding and Hoffmann published descriptions of Werdnig-Hoffmann disease in 1891. Hoffmann is also remembered for his 1897 descriptions of peroneal muscular atrophy and myopathy associated with hypothyroidism.

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Lillian M. Hudspeth Memorial Hospital (Sonora, Texas - Sutton County)