Whyte M P, Petersen D J, McAlister W H
Metabolic Research Unit, Shriners Hospital for Crippled Children, St. Louis, MO 63131.
Am J Med Genet. 1990 Jul;36(3):288-91. doi: 10.1002/ajmg.1320360308.
We describe a family with a new disorder characterized by congenital hypotrichosis and spondyloepimetaphyseal dysplasia that results in mild rhizomelic short stature. Five individuals in 3 generations are affected with autosomal dominant inheritance.