Rare hereditary diseases in newborns

E. V. Belogorskaya; Белогорская Е. В.; L. Ya. Alexandrova; Александрова Л. Я.; N. Kh. Gabitova; Габитова H. X.

doi:10.17816/kazmj65317

Rare hereditary diseases in newborns

Authors: Belogorskaya E.V.¹^,2, Alexandrova L.Y.¹^,2, Gabitova N.K.¹^,2
Affiliations:
1. S.V. Kurashov Kazan Medical Institute
2. 1st Children's Clinical Hospital of the city of Kazan
Issue: Vol 67, No 2 (1986)
Pages: 109-111
Section: Articles
URL: https://ogarev-online.ru/kazanmedj/article/view/65317
DOI: https://doi.org/10.17816/kazmj65317
ID: 65317

Cite item

Full Text

Abstract
Full Text
About the authors
References
Supplementary files
Statistics

Abstract

Pierre Robin syndrome is a rare disorder characterized by congenital facial malformations: microretrognathia, cleft soft or hard palate, microglossia, glossoptosis. In severe cases after birth, there is a threat of asphyxia of the newborn. The phenomena of glossoptosis usually diminish by 4 weeks of age.