Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Genet Couns ; 15(1): 27-36, 2004.
Article in English | MEDLINE | ID: mdl-15083696

ABSTRACT

Congenital brachial palsy is still a relatively common birth defect and almost a sporadic disorder. This work presents 2 unrelated Egyptian families; had several members in successive generations with severe unilateral congenital brachial palsy. Pedigree analysis of both families and the high rate of consanguinity among them are highly suggestive of autosomal recessive inheritance with variable expression.


Subject(s)
Myelin Proteins/genetics , Paresis/genetics , Child , Chromosomes, Human, X/genetics , Electromyography , Female , Humans , Male , Paresis/diagnosis , Paresis/physiopathology , Pedigree , Upper Extremity/innervation , Upper Extremity/physiopathology
SELECTION OF CITATIONS
SEARCH DETAIL
...