Genomic imprinting disorders in the structure of syndromic obesity in children

BACKGROUND. Genomic imprinting disorders represent a distinct class of hereditary diseases caused by disruption of the monoallelic expression of imprinted genes. Several of them are closely associated with obesity and metabolic disturbances. Syndromes such as Prader–Willi, Angelman, Schaaf–Yang, Tem...

Popoln opis

Bibliografske podrobnosti

Principais autores:	O. V. Vasyukova, E. P. Atavina-Ermakova, E. G. Panchenko, D. A. Kopytina, O. A. Simonova, V. Y. Udalova, I. V. Kanivets, D. B. Akimova, M. Y. Skoblov, M. A. Andreeva, E. V. Nagaeva, N. G. Mokrysheva
Format:	Artigo
Jezik:	Inglês
Izdano:	Endocrinology Research Centre 2025-12-01
Serija:	Ожирение и метаболизм
Teme:	genomic imprinting disorders prader–willi syndrome angelman syndrome schaaf–yang syndrome temple syndrome pseudohypoparathyroidism type 1a pseudohypoparathyroidism type 1b syndromic obesity
Online dostop:	https://www.omet-endojournals.ru/jour/article/view/13276
Oznake:	Označite Brez oznak, prvi označite!