CLINICAL CASE OF CHROMOSOME 22Q11.2 DELETION SYNDROME (DI-GEORGIE SYNDROME)
A clinical case of orphan genetic pathology – Di Georgi syndrome in a child in the neonatal period is presented. The complexity of timely diagnosis of this complication is demonstrated.
Main Authors: | Ирина Анатольевна Никитина, Елена Глебовна Цой, Светлана Владимировна Цигельник, Вадим Гельевич Мозес, Светлана Ивановна Елгина, Елена Владимировна Рудаева |
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Format: | Article |
Language: | Russian |
Published: |
The Publishing House Medicine and Enlightenment
2020-02-01
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Series: | Мать и дитя в Кузбассе |
Subjects: | |
Online Access: | http://mednauki.ru/index.php/MD/article/view/419 |
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