RARE DISEASE CORNELIA DE LANGE SYNDROME: DIAGNOSTIC CRITERIA. CASE FROM  PRACTICE

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DC Field	Value	Language
dc.contributor.author	Saidkhonova A.M., Mirrakhimova M.Kh.	-
dc.date.accessioned	2025-12-16T05:45:25Z	-
dc.date.available	2025-12-16T05:45:25Z	-
dc.date.issued	2025	-
dc.identifier.issn	2181-7812	-
dc.identifier.uri	http://repo.tma.uz/xmlui/handle/1/2668	-
dc.description.abstract	Cornelia de Lange syndrome is an archetypical genetic syndrome that is characterized by intellectual disability, well-defined facial features, upper limb anomalies and atypical growth, among numerous other signs and symp toms. This article describes the the clinical observation of a 6-year-old patient treated with the diagnosis of Corne lius de Lange syndrome in the multidisciplinary clinic of the Tashkent Medical Academy.	en_US
dc.language.iso	other	en_US
dc.publisher	O'zbekiston, Toshkent	en_US
dc.relation.ispartofseries	UDK;616-008.6-056.7	-
dc.subject	Cornelia de Lange syndrome, clinical ob servation, children, multiple malformations, pneumonia, Amsterdam dwarfism, Brahman de Lange syndrome	en_US
dc.title	RARE DISEASE CORNELIA DE LANGE SYNDROME: DIAGNOSTIC CRITERIA. CASE FROM PRACTICE	en_US
dc.type	Article	en_US
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