Congenital stridor with feeding difficulty as a presenting symptom of Dok7 congenital myasthenic syndrome.
OBJECTIVE: The congenital myasthenic syndromes (CMS) are a group of genetic disorders of neuromuscular transmission causing fatigable weakness. Symptoms may be present from birth, but diagnosis is often delayed for several years, notably in post-synaptic CMS due to mutations in the DOK7 gene. Recent...
المؤلفون الرئيسيون: | Jephson, C, Mills, N, Pitt, M, Beeson, D, Aloysius, A, Muntoni, F, Robb, SA, Bailey, C |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2010
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مواد مشابهة
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