Congenital non-progressive peripheral neuropathy with arthrogryposis multiplex.
نویسندگان
چکیده
A family is described in which a hereditary peripheral neuropathy occurs, inherited as an autosomal dominant character. The syndrome is present at birth and does not show any significant progression thereafter. Three of the cases have suffered from arthrogryposis multiplex congenita. A secondary myopathy is also present. The condition appears to be intermediary between peroneal muscular atrophy and Friedreich's ataxia. Appearance at birth, presence of arthrogryposis multiplex congenita, and the non-progressive nature separate it sharply from the other heredofamilial ataxias and peripheral neuropathies.
منابع مشابه
[Peripheral ischaemia after chronic ergot poisoning].
4. Robertson WL, Glinski LP, Kirkpatrick SJ, Pauli RM. Further evidence that arthrogryposis multiplex congenita in the human sometimes is caused by an intrauterine vascular accident. Teratology. 1992;45:345-51. 5. Aspelund G, Langer JC. Abdominal wall defects. Curr Paediatr. 2006;16:192-8. 6. Lam PK, Torfs CP. Interaction between maternal smoking and malnutrition in infant risk of gastroschisis...
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ورودعنوان ژورنال:
- Journal of neurology, neurosurgery, and psychiatry
دوره 37 3 شماره
صفحات -
تاریخ انتشار 1974