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Publikováno v:
Journal of Nature and Science of Medicine, Vol 5, Iss 3, Pp 309-312 (2022)
Pallister–Hall syndrome (PHS) is a rare, autosomal dominant genetic disorder. The phenotypic features of the syndrome include hypothalamic hamartoma, polydactyly, craniofacial anomalies, and other malformations. This case report describes a 5-year-
Externí odkaz:
https://doaj.org/article/85e5718a3673427ba69eea84d1ffa3fa