Journal article
Melanocortin‐4 Receptor Deficiency Phenotype with an Interstitial 18q Deletion: A Case Report of Severe Childhood Obesity and Tall Stature
Abstract
Childhood obesity is a growing health concern, associated with significant physical and psychological morbidity. Childhood obesity is known to have a strong genetic component, with mutations in the melanocortin-4 receptor (MC4R) gene being the most common monogenetic cause of obesity. Over 166 different MC4R mutations have been identified in persons with hyperphagia, severe childhood obesity, and increased linear growth. However, it is unclear …
Authors
Abdullah S; Reginold W; Kiss C; Harrison KJ; MacKenzie JJ
Journal
Case Reports in Pediatrics, Vol. 2016, No. 1,
Publisher
Hindawi
Publication Date
2016
DOI
10.1155/2016/6123150
ISSN
2090-6803