Please use this identifier to cite or link to this item: http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/16125
Title: PRADER-WILLI SYNDROME, DIAGNOSTICS AND CURRENCY FEATURES
Authors: Riznichuk, M.
Galitskaya, V.
Dyhodyuk, Yu.
Kravchuk, Yu.
Vakaryuk, Yu.
Keywords: Prader-Willi syndrome
obesity
children
hypogonadism
Issue Date: 2017
Publisher: Deutscher Wissenschaftsherold • German Science Herald
Series/Report no.: N4;p. 50-51
Abstract: Five boys with Prader-Willi syndrome were examined at the endocrinologist by 2016. All children had minimal diagnostic signs of the syndrome, namely: muscular hypotension, hypogonadism, obesity, mental retardation of varying severity, small hands and feet. In two children there was a disruption of glucose tolerance. All patients had the manifestation of hypergonadotropic hypogonadism. If a minimal diagnostic criteria are found in the newborn, a genetic analysis is necessary.
URI: http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/16125
Appears in Collections:Статті. Кафедра педіатрії та медичної генетики

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