Cleidocranial Dysplasia Affecting Three Generations in a Family: A Unique Case Report
Cleidocranial Dysplasia (CCD) is a rare autosomal dominant syndrome that occurs in approximately 1 per million individuals worldwide. This syndrome is characterized by skeletal, orofacial, and dental manifestations like hypoplastic or aplastic clavicle, shoulder hypermobility,...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Krishna Vishwa Vidyapeeth (Deemed to be University), Karad
2021-04-01
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| Col·lecció: | Journal of Krishna Institute of Medical Sciences University |
| Matèries: | |
| Accés en línia: | https://www.jkimsu.com/jkimsu-vol10no2/JKIMSU,%20Vol.%2010,%20No.%202,%20April-June%202021%20Page%20150-155.pdf |
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