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Phenotype of cranioectodermal dysplasia with different hair and bone abnormalities

 

作者: Edward J. Lammer,   Howard Baden,   Randall J. Margolis,  

 

期刊: American Journal of Medical Genetics  (WILEY Available online 1993)
卷期: Volume 45, issue 1  

页码: 9-13

 

ISSN:0148-7299

 

年代: 1993

 

DOI:10.1002/ajmg.1320450105

 

出版商: Wiley Subscription Services, Inc., A Wiley Company

 

关键词: ectodermal dysplasia;cranioectodermal dysplasia;bone dysplasia;craniosynostosis;hair follicle

 

数据来源: WILEY

 

摘要:

AbstractWe report on a 3‐year‐old boy with hair abnormalities and a generalized bone dysplasia. He had very short, sparse hair and craniosynotosis. His stature, growth, and limb lengths were normal, as was his neurological development. While this phenotype has some resemblance to cranioectodermal dysplasia, the radiographic and hair abnormalities are different. Histological studies showed abnormalities in the internal root sheath of the hair follicle and the hair shaft. These findings define a new ectodermal dysplasia syndrome of unknown cause. © 1993 Wiley‐Lis

 

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