THE CORNELIA DE LANGE SYNDROME (CASE STUDY)

Journal: Science Journal "NovaInfo" (Vol.2, No. 47)

Publication Date: 2016-06-16

Authors : Efimenko Oksana Vladimirovna; Knyazheva Elena Dmitrievna; Khonkeldieva Khurmatoy Kamchievna;

Page : 273-275

Keywords : MULTIPLE ANOMALIES IN THE DEVELOPMENT OF MENTAL RETARDATION; CORNELIA DE LANGE SYNDROME;

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Abstract

The Cornelia De Lange syndrome is a rare hereditary disease, according to the literature, occurs with a frequency of 1 to 30 thousand newborns. Feature of the disease is that, you can identify multiple anomalies in the development and later mental retardation with the child from birth.One caseof Cornelia De Lange in a 2year-old child.

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THE CORNELIA DE LANGE SYNDROME (CASE STUDY)

Abstract

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