Obesity and facial dysmorphism in an adolescent patient with a 16p11.2 microdeletion
A 17-year-old mixed race male has been followed in our adolescent clinic for severe obesity, dysmorphic features, and behavioral issues. Among other interventions, he has received symptomatic treatment for hypertension, insulin resistance, and attention deficit hyperactivity disorder. Genetic invest...
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Published in | International journal of adolescent medicine and health Vol. 30; no. 2; pp. 1066 - 1069 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Germany
De Gruyter
09.07.2016
Walter de Gruyter GmbH |
Subjects | |
Online Access | Get full text |
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Summary: | A 17-year-old mixed race male has been followed in our adolescent clinic for severe obesity, dysmorphic features, and behavioral issues. Among other interventions, he has received symptomatic treatment for hypertension, insulin resistance, and attention deficit hyperactivity disorder. Genetic investigation identified a 16p11.2 microdeletion, commonly associated with severe obesity and developmental delay. We present the clinical history, treatment, and implications for this patient. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2191-0278 0334-0139 2191-0278 |
DOI: | 10.1515/ijamh-2016-0041 |