Steinert disease


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Related to Steinert disease: Proximal myotonic myopathy

my·o·ton·ic dys·tro·phy

[MIM*160900]
the most common adult muscular dystrophy, characterized by progressive muscle weakness and wasting of some of the cranial innervated muscles, as well as the distal limb muscles; other clinical features include myotonia, cataracts, hypogonadism, cardiac abnormalities, and frontal balding; onset usually in the the third decade; autosomal dominant inheritance caused by abnormal trinucleotide repeat expansion in the dystrophia myotonica protein kinase gene (DMPK) on chromosome 19q. This disorder demonstrates anticipation (increase in severity in successive generations because of successive amplification of the trinucleotide repeats); the severe congenital form is almost always confined to the children of affected women.
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Steinert disease

(stin'ert)
[Hans Gustav Wilhelm Steinert, Ger. physician, 1875–1911]
Myotonia dystrophica.
Medical Dictionary, © 2009 Farlex and Partners

Steinert,

(Steinhert), Hans, German physician, 1875–.
Curschmann-Batten-Steinert syndrome - see under Curschmann
Steinert disease - a chronic, slowly progressing disease marked by atrophy of the muscles, failing vision, lenticular opacities, ptosis, slurred speech, and general muscular weakness. Synonym(s): myotonic dystrophy
Steinert myotonic dystrophy
Steinert syndrome
Medical Eponyms © Farlex 2012