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. 1980 Jun;72(6):597–599.

Chondroectodermal Dysplasia in an African Child: A Case Report

Noel Guillozet, Joseph Mbede
PMCID: PMC2552454  PMID: 7392080

Abstract

Chondroectodermal dysplasia is a rare autosomal recessive disorder characterized by short extremities, short stature, polydactyly, and nail hypoplasia. Dental abnormalities, congenital heart defects, and thoracic abnormalities impending respiration are seen in many patients. Virtually all previous reports of the classic disorder have been in Caucasians. In the following case report, chondroectodermal dysplasia is described in a black Cameroonian infant.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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