Rare case of orofaciodigital syndrome type I

Orofaciodigital syndrome (OFDS) is a group of congenital anomalies which affects the face, oral structures and digits. There are nine subtypes with different modes of inheritance. OFDS type I is an X-linked dominant trait with lethality in the vast majority of affected males. We report a case of OFD...

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Hlavní autoři: Singh, Abhishek Bahadur, Girhotra, Manish, Goel, Medha, Bhatia, Shilpee
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Publishing Group 2013
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3604300/
https://ncbi.nlm.nih.gov/pubmed/23417374
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2012-007733
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