Weaver syndrome in a 16-year-old child (clinical case description)

In their practice, pediatricians often observes patients with significant disorders in their physical development. In most cases, these changes are related to dwarfism and quite often conditioned by hereditary factors. But special attention should be paid to children with high anthropometric paramet...

Full description

Saved in:
Bibliographic Details
Main Authors: T. A. Bokova, D. A. Kartashova, Yu. Yu. Kotalevskaya
Format: Article
Language:Russian
Published: Open Systems Publication 2021-06-01
Series:Лечащий Врач
Subjects:
Online Access:https://journal.lvrach.ru/jour/article/view/657
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849248404356464640
author T. A. Bokova
D. A. Kartashova
Yu. Yu. Kotalevskaya
author_facet T. A. Bokova
D. A. Kartashova
Yu. Yu. Kotalevskaya
author_sort T. A. Bokova
collection DOAJ
description In their practice, pediatricians often observes patients with significant disorders in their physical development. In most cases, these changes are related to dwarfism and quite often conditioned by hereditary factors. But special attention should be paid to children with high anthropometric parameters. The article presents a case of own observation of extremely rare combination of tallness and congenital disorders in development – Weaver syndrome in a 16-year-old adolescent.
format Article
id doaj-art-e55431445f3b4640bfcf8ee9c964c23e
institution Kabale University
issn 1560-5175
2687-1181
language Russian
publishDate 2021-06-01
publisher Open Systems Publication
record_format Article
series Лечащий Врач
spelling doaj-art-e55431445f3b4640bfcf8ee9c964c23e2025-08-20T03:57:51ZrusOpen Systems PublicationЛечащий Врач1560-51752687-11812021-06-0101656Weaver syndrome in a 16-year-old child (clinical case description)T. A. Bokova0D. A. Kartashova1Yu. Yu. Kotalevskaya2ГБУЗ МО МОНИКИ им. М. Ф. ВладимирскогоГБУЗ МО МОНИКИ им. М. Ф. ВладимирскогоГБУЗ МО МОНИКИ им. М. Ф. ВладимирскогоIn their practice, pediatricians often observes patients with significant disorders in their physical development. In most cases, these changes are related to dwarfism and quite often conditioned by hereditary factors. But special attention should be paid to children with high anthropometric parameters. The article presents a case of own observation of extremely rare combination of tallness and congenital disorders in development – Weaver syndrome in a 16-year-old adolescent.https://journal.lvrach.ru/jour/article/view/657tallnessgeneticschildrencongenital disease
spellingShingle T. A. Bokova
D. A. Kartashova
Yu. Yu. Kotalevskaya
Weaver syndrome in a 16-year-old child (clinical case description)
Лечащий Врач
tallness
genetics
children
congenital disease
title Weaver syndrome in a 16-year-old child (clinical case description)
title_full Weaver syndrome in a 16-year-old child (clinical case description)
title_fullStr Weaver syndrome in a 16-year-old child (clinical case description)
title_full_unstemmed Weaver syndrome in a 16-year-old child (clinical case description)
title_short Weaver syndrome in a 16-year-old child (clinical case description)
title_sort weaver syndrome in a 16 year old child clinical case description
topic tallness
genetics
children
congenital disease
url https://journal.lvrach.ru/jour/article/view/657
work_keys_str_mv AT tabokova weaversyndromeina16yearoldchildclinicalcasedescription
AT dakartashova weaversyndromeina16yearoldchildclinicalcasedescription
AT yuyukotalevskaya weaversyndromeina16yearoldchildclinicalcasedescription