Auralcephalosyndactyly

Common Name(s)

Auralcephalosyndactyly, Kurczynski Casperson 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 "Auralcephalosyndactyly" 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 "Auralcephalosyndactyly" returned 2 free, full-text research articles on human participants. First 3 results:

Auralcephalosyndactyly: a new craniosynostosis syndrome or a variant of the Saethre-Chotzen syndrome?
 

Author(s): E Legius, J P Fryns, H Van den Berghe

Journal: J. Med. Genet.. 1989 Aug;26(8):522-4.

 

A mother and son are reported with bilateral, symmetrical syndactyly of the third, fourth, and fifth toes, mild craniosynostosis of the coronary sutures, and small pinnae. The same combination of malformations was recently described as a new syndrome by Kurczynsky and Casperson in ...

Last Updated: 3 Oct 1989

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Auralcephalosyndactyly: a new hereditary craniosynostosis syndrome.
 

Author(s): T W Kurczynski, S M Casperson

Journal: J. Med. Genet.. 1988 Jul;25(7):491-3.

 

A family is described in which craniosynostosis is associated with characteristic pinnae, a short columella, and symmetrical syndactyly of the fourth and fifth toes, inherited as an autosomal dominant condition. Various dominantly inherited syndromes involving craniosynostosis have ...

Last Updated: 17 Nov 1988

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Reviews from the PubMed Database

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Symptoms, Diagnosis, and Treatment

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