Oculoectodermal syndrome

Common Name(s)

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

Oculoectodermal syndrome: twentieth described case with new manifestations.
 

Author(s): Daniela de Almeida Figueiras, Deborah Maria de Castro Barbosa Leal, Valter Kozmhinsky, Marina Coutinho Domingues Querino, Marina Genesia da Silva Regueira, Maria Gabriela de Morais Studart

Journal: An Bras Dermatol. ;91(5 suppl 1):160-162.

 

Oculoectodermal syndrome is a rare disease characterized by the association of aplasia cutis congenita, epibulbar dermoids, and other abnormalities. This report describes the twentieth case of the disease. We report a 4-year-old female child who presented with the classical features ...

Last Updated: 31 Dec 1969

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Reviews from the PubMed Database

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The terms "Oculoectodermal syndrome" 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.