PRADER-WILLI SYNDROME, DIAGNOSTICS AND CURRENCY FEATURES

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DC Field	Value	Language
dc.contributor.author	Riznichuk, M.
dc.contributor.author	Galitskaya, V.
dc.contributor.author	Dyhodyuk, Yu.
dc.contributor.author	Kravchuk, Yu.
dc.contributor.author	Vakaryuk, Yu.
dc.date.accessioned	2020-10-19T12:17:42Z
dc.date.available	2020-10-19T12:17:42Z
dc.date.issued	2017
dc.identifier.uri	http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/16125
dc.description.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.	uk_UA
dc.publisher	Deutscher Wissenschaftsherold • German Science Herald	uk_UA
dc.relation.ispartofseries	N4;p. 50-51
dc.subject	Prader-Willi syndrome	uk_UA
dc.subject	obesity	uk_UA
dc.subject	children	uk_UA
dc.subject	hypogonadism	uk_UA
dc.title	PRADER-WILLI SYNDROME, DIAGNOSTICS AND CURRENCY FEATURES	uk_UA
dc.type	Article	uk_UA
Appears in Collections:	Статті. Кафедра педіатрії та медичної генетики

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