Syndactyly type 2

Common Name(s)

Syndactyly type 2

Description for this condition is not yet available.
 

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Condition Specific Organizations

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Syndactyly type 2" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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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 "Syndactyly type 2" returned 1 free, full-text research articles on human participants. First 3 results:

A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?
 

Author(s): A N Akarsu, O Akhan, B S Sayli, U Sayli, G Baskaya, M Sarfarazi

Journal: J. Med. Genet.. 1995 Jun;32(6):435-41.

 

Syndactyly type II (synpolydactyly (SPD)) is an autosomal dominant condition with typical abnormalities of the distal parts of both upper and lower limbs. We report here a previously undescribed phenotypic feature of people with severe hand and foot deformities who were born to two ...

Last Updated: 12 Oct 1995

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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 "Syndactyly type 2" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.