Ectodermal dysplasias: a clinical classification and a causal review

Am J Med Genet. 1994 Nov 1;53(2):153-62. doi: 10.1002/ajmg.1320530207.

Abstract

We present a casual review of 154 ectodermal dysplasias (EDs) as classified into 11 clinical subgroups. The number of EDs in each subgroup varies from one to 43. The numbers of conditions due to autosomal dominant, autosomal recessive, and X-linked genes are, respectively, 41, 52, and 8. In 53 conditions cause is unknown; 35 of them present some causal (genetic) suggestion.

Publication types

  • Review

MeSH terms

  • Chromosome Mapping
  • Ectodermal Dysplasia / classification*
  • Ectodermal Dysplasia / etiology
  • Ectodermal Dysplasia / genetics*
  • Female
  • Genes, Dominant
  • Genes, Recessive
  • Genetic Linkage
  • Humans
  • Male
  • X Chromosome