Fuhrmann Syndrome

Common Name(s)

Fuhrmann Syndrome

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Fuhrmann Syndrome" 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 "Fuhrmann Syndrome" returned 1 free, full-text research articles on human participants. First 3 results:

Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.
 

Author(s): C G Woods, S Stricker, P Seemann, R Stern, J Cox, E Sherridan, E Roberts, K Springell, S Scott, G Karbani, S M Sharif, C Toomes, J Bond, D Kumar, L Al-Gazali, S Mundlos

Journal: Am. J. Hum. Genet.. 2006 Aug;79(2):402-8.

 

Fuhrmann syndrome and the Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome are considered to be distinct limb-malformation disorders characterized by various degrees of limb aplasia/hypoplasia and joint dysplasia in humans. In families with these syndromes, we found homozygous ...

Last Updated: 31 Dec 1969

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Reviews from the PubMed Database

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The terms "Fuhrmann Syndrome" 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.