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Case Reports
. 1996 Jan 2;61(1):42-4.
doi: 10.1002/(SICI)1096-8628(19960102)61:1<42::AID-AJMG8>3.0.CO;2-Z.

Aplasia cutis congenita, high myopia, and cone-rod dysfunction in two sibs: a new autosomal recessive disorder

R Gershoni-Baruch  1 , R Leibo
Affiliations
Case Reports

Aplasia cutis congenita, high myopia, and cone-rod dysfunction in two sibs: a new autosomal recessive disorder

R Gershoni-Baruch et al. Am J Med Genet. .

Abstract

We report on a brother and a sister with congenital nystagmus, cone-rod dysfunction, high myopia, and aplasia cutis congenita on the midline of the scalp vertex. To our knowledge this familial oculocutaneous condition, transmitted as an autosomal recessive trait, has not been reported previously.

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