Familial congenital brachial palsy

Eight relatives in a Sicilian family, including a sibship of 5, were affected with severe unilateral congenital brachial palsy (CBP) in a pattern suggesting autosomal dominant inheritance with reduced penetrance (6 cases affected on the right, 2 on the left). X‐linked inheritance with expression in...

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Veröffentlicht in:	American journal of medical genetics 1991-12, Vol.41 (3), p.322-324
Hauptverfasser:	Mollica, F., Volti, S. Li, Grasso, A., De Simone, D.
Format:	Artikel
Sprache:	eng
Schlagworte:	Arm - abnormalities autosomal dominant inheritance Biological and medical sciences Brachial Plexus - physiopathology Diabetes Complications Diabetes Mellitus - genetics Female Genes, Dominant - genetics Humans inheritance macrosomla Male maternal diabetes mellitus Medical sciences Neurology Paralysis - complications Paralysis - congenital Paralysis - genetics Pedigree
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