J Med Genet. 1991 Aug;28(8):544-6.

Facial dysmorphism: a marker of autosomal dominant cranial diabetes insipidus.

Laing RB, Dean JC, Pearson DW, Johnston AW.

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Department of Clinical Genetics, Aberdeen Royal Infirmary.

Abstract

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.

PMID:: 1920373; [PubMed - indexed for MEDLINE]
PMCID:: PMC1016986

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