Facial dysmorphism: a marker of autosomal dominant cranial diabetes insipidus.
AUTOR(ES)
Laing, R B
RESUMO
We report a family with autosomal dominant cranial diabetes insipidus in which a characteristic facial appearance of hypertelorism, broad and prominent nasal bridge, short nose, and long philtrum is seen in affected members.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1016986Documentos Relacionados
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