Meckel syndrome type 3

Common Name(s)

Meckel syndrome type 3

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Meckel syndrome type 3" for support, advocacy or research.

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

A mouse model for Meckel syndrome type 3.
 

Author(s): Susan A Cook, Gayle B Collin, Roderick T Bronson, J├╝rgen K Naggert, Dong P Liu, Ellen C Akeson, Muriel T Davisson

Journal: J. Am. Soc. Nephrol.. 2009 Apr;20(4):753-64.

 

Meckel-Gruber syndrome type 3 (MKS3; OMIM 607361) is a severe autosomal recessive disorder characterized by bilateral polycystic kidney disease. Other malformations associated with MKS3 include cystic changes in the liver, polydactyly, and brain abnormalities (occipital encephalocele, ...

Last Updated: 30 Mar 2009

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Reviews from the PubMed Database

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The terms "Meckel syndrome type 3" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.