OF UNIPARENTAL DISOMY OR RUSSELL-SILVER SYNDROME

S.J. Bokonbaeva E.M. Mambetsadykova J.M. Sushanlo G.P. Aphanasenko A.S. Kadyrova E.G. Kim

DOI:

https://doi.org/10.54890/.v1i1(2).1105

Abstract

Resume. The article presents the main clinical and laboratory and genetic manifestations syndrome Russell - Silver caused of uniparental disomy of chromosome 7.

Keywords:

delayed physical development, dwarfism, facial dysmorphia, a sign of Dubois, of uniparental disomy

Author Biographies

S.J. Bokonbaeva, Kyrgyz-Russian Slavic University

Department of Pediatrics

E.M. Mambetsadykova, Kyrgyz-Russian Slavic University

Department of Pediatrics

J.M. Sushanlo, Kyrgyz-Russian Slavic University

Department of Pediatrics

G.P. Aphanasenko, Kyrgyz-Russian Slavic University

Department of Pediatrics

A.S. Kadyrova, Kyrgyz-Russian Slavic University

Department of Pediatrics

E.G. Kim, Kyrgyz-Russian Slavic University

Department of Pediatrics

References

1. Silver N.K: Asymmetry, short stature, and variations in sexual development: a syndrome of congenital malformations. Am. J. Dis. Child. 107: 495-515, 1964.

2. Хертл М. «Дифференциальная диагностика в педиатрии». Т.1: пер.с нем. - М. : Медицина, 1990. – 552 с.

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Published

2024-01-04

How to Cite

Боконбаева, С. ., Е. . Мамбетсадыкова, Х. Сушанло, Г. Афанасенко, А. . Кадырова, and Е. . Ким. “OF UNIPARENTAL DISOMY OR RUSSELL-SILVER SYNDROME”. Euroasian Health Journal, vol. 1, no. 1(2), Jan. 2024, pp. 70-72, doi:10.54890/.v1i1(2).1105.

Issue

Vol. 1 No. 1(2) (2015): VESTNIK of KSMA

Section

PEDIATRY
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