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Melanocortin‐4 Receptor Deficiency Phenotype with...
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