22q11.2 Deletion Syndrome: Symptoms, Diagnosis, Treatment

The article analyzes the consequences of chromosomal abnormalities caused by the deletion of a small piece of chromosome 22. This syndrome results in diverse clinical manifestations: congenital heart defects, abnormalities in the large vessels, congenital defects in the maxillofacial area, as well a...

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Détails bibliographiques
Auteurs principaux: Leyla S. Namazova-Baranova, Olga V. Ginter, Tatyana A. Polunina, Irina V. Davydova, Kirill V. Savostyanov, Alexandr A. Pushkov, Natalya V. Jourkova, Tatyana Y. Mospan
Format: Article
Langue:English
Publié: "Paediatrician" Publishers LLC 2016-12-01
Collection:Вопросы современной педиатрии
Sujets:
Accès en ligne:https://vsp.spr-journal.ru/jour/article/view/1697