Send to

Choose Destination
Am J Med Genet. 1996 Jan 2;61(1):42-4.

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

Author information

Department of Human Genetics, Rambam Medical Center, Haifa, Israel.


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.

Supplemental Content

Loading ...
Support Center