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J Med Genet 1991;28:544-546 doi:10.1136/jmg.28.8.544
  • Research Article

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

  1. R B Laing,
  2. J C Dean,
  3. D W Pearson,
  4. A W Johnston
  1. 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.

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