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pro vyhledávání: '"Abdulrahman M. Mohammad"'
Autor:
Hussein M. Alshamrani, Luai M. Assaedi, Jumanah A. Bahattab, Abdulrahman M. Mohammad, Magdy R. Abdulghani
Publikováno v:
Case Reports in Dermatological Medicine, Vol 2023 (2023)
LEOPARD syndrome (LS) is a rare autosomal dominant inherited or sporadic genetic disorder caused commonly by missense mutations in the protein-tyrosine phosphatase-nonreceptor type 11 (PTPN11) gene. Due to its rarity and a high chance of misdiagnosis
Externí odkaz:
https://doaj.org/article/5da48ace51c240b28032af105ccac66a