Autosomal recessive anhidrotic ectodermal dysplasia in a large Moroccan family.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 9863606.
- Also identified by PMC identifier 1051521.
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Abstract
We studied a large Moroccan family in which anhidrotic ectodermal dysplasia is transmitted as an autosomal recessive trait. Fourteen family members, both males and females, were affected and they all had a common ancestor. Linkage analysis by homozygosity mapping in this family will permit the gene localisation of this rare form of anhidrotic ectodermal dysplasia.
Medical subject headings
- Ectodermal Dysplasia
- Genes, Recessive