| Literature DB >> 16246000 |
Ali Al Kaissi1, Farid Ben Chehida, Nabil Nassib, Hatem Safi, Mrad Djnziri, Maher Ben Ghachem, Hassan Gharbi.
Abstract
We report an inbred Tunisian family, in which the proband manifested signs of hypohidrotic ectodermal dysplasia, subtotal amelia, scoliosis and left renal agenesis. Two other family members had the full clinical criteria of hypohidrotic ectodermal dysplasia, characterized by deficient sweat glands, hypodontia, hypoplasia of the mucous glands, and fine hair. Nine family subjects had variable clinical expression of the disorder.Entities:
Mesh:
Year: 2005 PMID: 16246000 PMCID: PMC1831925 DOI: 10.5555/afhs.2005.5.3.270
Source DB: PubMed Journal: Afr Health Sci ISSN: 1680-6905 Impact factor: 0.927