Rare hereditary diseases in newborns
E. V. Belogorskaya , L. Ya. Alexandrova , N. Kh. Gabitova
Kazan medical journal ›› 1986, Vol. 67 ›› Issue (2) : 109 -111.
Rare hereditary diseases in newborns
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.
Belogorskaya E.V., Alexandrova L.Y., Gabitova N.K.
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