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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.

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Bibliographic Details
Main Authors:	Ирина Анатольевна Никитина (Author), Елена Глебовна Цой (Author), Светлана Владимировна Цигельник (Author), Вадим Гельевич Мозес (Author), Светлана Ивановна Елгина (Author), Елена Владимировна Рудаева (Author)
Format:	Book
Published:	The Publishing House Medicine and Enlightenment, 2020-02-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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Description
Summary:	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.
Item Description:	1991-010X 2542-0968