Ectodermal Dysplasia 2, Hidrotic

Common Name(s)

Ectodermal Dysplasia 2, Hidrotic

Hidrotic ectodermal dysplasia 2, or Clouston sundrome, is a rare genetic disorder. People with hidrotic ectodermal dysplasia 2 usually have wiry, brittle, and pale hair with milky white nails when they are born. After a few years they begin to lose all their hair and in extreme cases may be completely bald by the time they enter puberty. Other symptoms of hidrotic ectodermal dysplasia 2 include degeneration of the nails, more pigment (color) in the skin over their joints, and clubbed fingers. Talk with your doctor to find the best treatment for you if you have been diagnosed with hidrotic ectodermal dysplasia 2.

Source: Advocacy organizations associated with the condition.

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Advocacy and Support Organizations Health Questions Recommended Apps Scientific Literature Symptoms, Diagnosis, and Treatment Clinical Trial Information
 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Ectodermal Dysplasia 2, Hidrotic" 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: 12 Feb 2018

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General Support Organizations

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How do you compare to others with this condition?

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Ectodermal Dysplasia 2, Hidrotic" 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: 12 Feb 2018

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General Support Organizations

Not finding the support you need? Show General Support Organizations

 
 
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Recommended Apps

Privately answer questions about your health. Let resources, you select, come to you

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.

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Relief is when you and the right researcher find each other

Finding the right clinical trial for Ectodermal Dysplasia 2, Hidrotic 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.

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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 "Ectodermal Dysplasia 2, Hidrotic" returned 0 free, full-text research articles on human participants.

No free, full-text research articles on human participants are available at this time. Please click this link to visit the PubMed website for results on "Ectodermal Dysplasia 2, Hidrotic".

Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Ectodermal Dysplasia 2, Hidrotic" 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 "Ectodermal Dysplasia 2, Hidrotic".

 
 
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Symptoms, Diagnosis, and Treatment

This information is provided by Genetics Home Reference.
https://ghr.nlm.nih.gov/condition/clouston-syndrome
https://ghr.nlm.nih.gov/gene/TUBA3C
https://ghr.nlm.nih.gov/condition/hypohidrotic-ectodermal-dysplasia
https://ghr.nlm.nih.gov/condition/oculodentodigital-dysplasia
https://ghr.nlm.nih.gov/gene/EDARADD
https://ghr.nlm.nih.gov/gene/EDA
https://ghr.nlm.nih.gov/gene/EDAR
https://ghr.nlm.nih.gov/condition/cranioectodermal-dysplasia
https://ghr.nlm.nih.gov/gene/NECTIN1
https://ghr.nlm.nih.gov/condition/atelosteogenesis-type-2
https://ghr.nlm.nih.gov/condition/otopalatodigital-syndrome-type-2
https://ghr.nlm.nih.gov/condition/anhidrotic-ectodermal-dysplasia-with-immune-deficiency
https://ghr.nlm.nih.gov/gene/TP63
https://ghr.nlm.nih.gov/gene/KCTD1
https://ghr.nlm.nih.gov/gene/PKP1
https://ghr.nlm.nih.gov/gene/GJB6
https://ghr.nlm.nih.gov/condition/ankyloblepharon-ectodermal-defects-cleft-lip-palate-syndrome
https://ghr.nlm.nih.gov/gene/NFKBIA
https://ghr.nlm.nih.gov/gene/WDR19
https://ghr.nlm.nih.gov/gene/IKBKG
Full Results at Genetics Home Reference: 1355 matches

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.

According to ClinicalTrials.gov there are currently 0 additional "open" studies for "Ectodermal Dysplasia 2, Hidrotic" (open studies are recruiting volunteers) and 0 "Ectodermal Dysplasia 2, Hidrotic" studies with "all" status. Visit ClinicalTrials.gov now to view them. Or alternatively, consider TrialsFinder for assistance:
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Relief is when you and the right researcher find each other
Finding the right clinical trial for Ectodermal Dysplasia 2, Hidrotic 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.
Learn More