Hypohidrotic ectodermal dysplasia autosomal recessive

Common Name(s)

Hypohidrotic ectodermal dysplasia autosomal recessive

Description for this condition is not yet available.
 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Hypohidrotic ectodermal dysplasia autosomal recessive" for support, advocacy or research.

National Foundation for Ectodermal Dysplasias

The National Foundation for Ectodermal Dysplasias’ mission is to empower and connect people touched by ectodermal dysplasias through education, support, and research.

Last Updated: 7 May 2014

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Hypohidrotic ectodermal dysplasia autosomal recessive" for support, advocacy or research.

National Foundation for Ectodermal Dysplasias

The National Foundation for Ectodermal Dysplasias’ mission is to empower and connect people touched by ectodermal dysplasias through education, support, and research.

http://www.nfed.org

Last Updated: 7 May 2014

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Hypohidrotic ectodermal dysplasia autosomal recessive" returned 2 free, full-text research articles on human participants. First 3 results:

Subtotal amelia in a child with autosomal recessive hypohidrotic ectodermal dysplasia.
 

Author(s): Ali Al Kaissi, Farid Ben Chehida, Nabil Nassib, Hatem Safi, Mrad Djnziri, Maher Ben Ghachem, Hassan Gharbi

Journal: Afr Health Sci. 2005 Sep;5(3):270-5.

 

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 ...

Last Updated: 25 Oct 2005

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Definitive evidence for an autosomal recessive form of hypohidrotic ectodermal dysplasia clinically indistinguishable from the more common X-linked disorder.
 

Author(s): F Munoz, G Lestringant, V Sybert, M Frydman, A Alswaini, P M Frossard, R Jorgenson, J Zonana

Journal: Am. J. Hum. Genet.. 1997 Jul;61(1):94-100.

 

A crucial issue in genetic counseling is the recognition of nonallelic genetic heterogeneity. Hypohidrotic (anhidrotic) ectodermal dysplasia (HED), a genetic disorder characterized by defective development of hair, teeth, and eccrine sweat glands, is usually inherited as an X-linked ...

Last Updated: 26 Aug 1997

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Hypohidrotic ectodermal dysplasia autosomal recessive" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

There are currently no related results available in GeneReviews.

There are currently no related results available in Genetic Testing Registry.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.