Tel Hashomer camptodactyly syndrome

Common Name(s)

Tel Hashomer camptodactyly 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 "Tel Hashomer camptodactyly 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 "Tel Hashomer camptodactyly syndrome" returned 2 free, full-text research articles on human participants. First 3 results:

Tel Hashomer camptodactyly syndrome: report of a case with myopathic features.
 

Author(s): M A Patton, K D McDermot, B D Lake, M Baraitser

Journal: J. Med. Genet.. 1986 Jun;23(3):268-71.

 

A child with the Tel Hashomer camptodactyly syndrome is reported. Although muscle weakness and hypoplasia are reported features of this syndrome, further investigation of muscle function has not previously been carried out. We report a raised creatine kinase and an abnormal electromyogram ...

Last Updated: 25 Jul 1986

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Camptodactyly, with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases: Tel Hashomer camptodactyly syndrome.
 

Author(s): R M Goodman, M B Katznelson, M Hertz, A Katznelson

Journal: J. Med. Genet.. 1976 Apr;13(2):136-41.

 

A syndrome characterized by camptodactyly, distinct facial features, multiple musculoskeletal defects, and unique dermatoglyphic changes is described in two sisters born of consanguineous parents. In 1972 this same constellation of findings was first reported in two sibs from a different ...

Last Updated: 23 Aug 1976

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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 "Tel Hashomer camptodactyly syndrome" returned 1 free, full-text review articles on human participants. First 3 results:

The status of dermatoglyphics as a biomarker of Tel Hashomer camptodactyly syndrome: a review of the literature.
 

Author(s): Buddhika T B Wijerathne, Robert J Meier, Suneth B Agampodi

Journal:

 

Tel Hashomer camptodactyly syndrome is a rare disease and only a few cases have been reported. Dermatoglyphics potentially provide relevant phenotypic biomarkers that were initially noted as a vital clinical feature of this disease. Dermatoglyphics possibly can indicate growth disturbances ...

Last Updated: 21 Sep 2016

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Clinical Trial Information This information is provided by ClinicalTrials.gov

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