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pro vyhledávání: '"Aya S. Hegazy"'
Autor:
Magd A. Kotb, Fatma Al Zahraa Mostafa, Ahmed M. Badr, Aya S. Hegazy, Mohamed S. Eid, Nahla I. Sabry, Radwa Shamma
Publikováno v:
Pediatric Sciences Journal, Vol 2, Iss 1, Pp 72-81 (2022)
Background: Wilson disease (WD) is an autosomal recessive disease with copper overload. Its clinical picture depends on specific tissue/system damage by the excess copper. Aim of the work: We aimed to study prospectively the phenotypic spectrum of s
Externí odkaz:
https://doaj.org/article/0a04f3c75e7f41b58cabe4c625f21845
