Bazsites.com Ectodermal Dysplasia

Directory Topics

NORD: Ectodermal Dysplasias - Offers synonyms, a general discussion and resources.
National Foundation for Ectodermal Dysplasia - ED organization based in North America offering information/advice to individuals and supporting scientific research. Includes a newsletter, publications, FAQs and a list of services.
Ectodermal Dysplasia Society - Information about the organization as well as the ED condition. Includes links, news articles and contact details.
The Ectodermal Dysplasia Mailing List - Includes instructions on joining the list, FAQs and links to further resources.
The Andy Fund - Describes the health condition of a boy who was born with ectodermal dysplasia with immune deficiency caused by a mutation on the fourth part of the NEMO gene.
The CaF Directory - Information about the ectodermal dysplasia disorders, the inheritance patterns and pre-natal diagnosing.
The Experimental Ophthalmology Unit - Research and teaching centre for the control and treatment of eye disorders and our interests include ARMD, corneal scarring, diabetes, ectodermal dysplasia, genetics, glaucoma, melanoma and PVR.

Hypohidrotic ectodermal dysplasia - Hypohidrotic ectodermal dysplasia is one of about 150 types of ectodermal dysplasia in humans. Before birth, these disorders result in the abnormal development of structures including the skin, hair, nails, teeth, and sweat glands.
Hay-Wells syndrome - Hay-Wells Syndrome (HWS), also known as the ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome, is one of at least 150 known types of ectodermal dysplasia. These syndromes affect tissues that arise from ectoderm, especially skin, hair, and nails.
TP73L - TP73L is a protein associated with ectrodactyly-ectodermal dysplasia-cleft syndrome.
AREDYLD - AREDYLD stands for "acral renal ectodermal dysplasia lipoatrophic diabetes." AREDLYD is categorized as a "rare" disease, meaning it affects fewer than 200,000 people in the American population.
Zadik Barak Levin syndrome - Zadik Barak Levin Syndrome (ZBLS) is a congenital disorder in humans. Presenting conditions include primary hypothyroidism, cleft palate, hypodontia, and ectodermal dysplasia.