Hypohidrotic ectodermal dysplasia autosomal dominant
Common Name(s)
Hypohidrotic ectodermal dysplasia autosomal dominant
Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "Hypohidrotic ectodermal dysplasia autosomal dominant" for support, advocacy or research.
The National Foundation for Ectodermal Dysplasias’ mission is to empower and connect people touched by ectodermal dysplasias through education, support, and research.
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Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "Hypohidrotic ectodermal dysplasia autosomal dominant" for support, advocacy or research.
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.orgRecommended Apps
Anonymously share and see how your answers compare with others with this condition while privately providing key pieces of information to medical researchers, disease advocacy groups, and others ONLY YOU select to help speed up cures and better alternatives.
Finding the right clinical trial for Hypohidrotic ectodermal dysplasia autosomal dominant can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.
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 dominant" returned 3 free, full-text research articles on human participants.
First 3 results:
Journal: Arch Argent Pediatr. 2017 02;115(1):e34-e38.
Hypohidrotic ectodermal dysplasia (HED) is a rare disease characterized by deficiency in development of structure derived from the ectoderm and is caused by mutations in the genes EDA, EDAR, or EDARADD. Phenotypes caused by mutations in these three may exhibit similar clinical features, ...
Journal:
Hypohidrotic ectodermal dysplasia (HED) is a genetic disorder characterized by defective development of teeth, hair, nails and eccrine sweat glands. Both autosomal dominant and autosomal recessive forms of HED have previously been linked to mutations in the ectodysplasin 1 anhidrotic ...
Journal: Am. J. Hum. Genet.. 1998 May;62(5):1102-6.
Autosomal dominant hypohidrotic ectodermal dysplasia (ADHED) is a disorder characterized by fine, slow-growing scalp and body hair, sparse eyebrows and eyelashes, decreased sweating, hypodontia, and nail anomalies. By genetic linkage analysis of a large ADHED kindred, we have mapped ...
To view other free, full-text articles on human participants, please click on the link below.
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 dominant" returned 0 free, full-text review articles on human participants.
No free, full-text review articles on human participants are available at this time. Please click this link to visit the PubMed website for results on "Hypohidrotic ectodermal dysplasia autosomal dominant".
Symptoms, Diagnosis, and Treatment
https://ghr.nlm.nih.gov/gene/EDARADD
https://ghr.nlm.nih.gov/gene/EDAR
https://ghr.nlm.nih.gov/condition/anhidrotic-ectodermal-dysplasia-with-immune-deficiency
https://ghr.nlm.nih.gov/gene/EDA
https://ghr.nlm.nih.gov/condition/oculodentodigital-dysplasia
https://ghr.nlm.nih.gov/condition/craniometaphyseal-dysplasia
https://ghr.nlm.nih.gov/condition/clouston-syndrome
https://ghr.nlm.nih.gov/condition/autosomal-dominant-hypocalcemia
https://ghr.nlm.nih.gov/condition/autosomal-dominant-vitreoretinochoroidopathy
https://ghr.nlm.nih.gov/condition/cranioectodermal-dysplasia
https://ghr.nlm.nih.gov/gene/TP63
https://ghr.nlm.nih.gov/condition/ankyloblepharon-ectodermal-defects-cleft-lip-palate-syndrome
https://ghr.nlm.nih.gov/condition/autosomal-dominant-hyper-ige-syndrome
https://ghr.nlm.nih.gov/gene/KRT14
https://ghr.nlm.nih.gov/gene/KCTD1
https://ghr.nlm.nih.gov/condition/multiple-epiphyseal-dysplasia
https://ghr.nlm.nih.gov/gene/NECTIN4
https://ghr.nlm.nih.gov/condition/scalp-ear-nipple-syndrome
https://ghr.nlm.nih.gov/gene/PKP1
Clinical Trial Information This information is provided by ClinicalTrials.gov
There are currently no open clinical trials for this condition.
Finding the right clinical trial for Hypohidrotic ectodermal dysplasia autosomal dominant can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.