Unexpected endocrine features and normal pigmentation in a young adult patient carrying a novel homozygous mutation in the POMC gene

Karine Clément, Béatrice Dubern, Monica Mencarelli, Paul Czernichow, Shosuke Ito, Kazumasa Wakamatsu, Gregory S. Barsh, Christian Vaisse, Juliane Leger

Research output: Contribution to journalArticle

53 Citations (Scopus)

Abstract

Context: Proopiomelanocortin (POMC) is the precursor to five biologically active peptides, including ACTH produced in the anterior pituitary and α-MSH produced in the hypothalamus. Mutations that inactivate the POMC gene have been described in children, causing a pleiotropic syndrome that includes secondary hypocortisolism, severe obesity, and variable changes in skin and hair pigmentation. Objective: We describe a female patient of North African ancestry, homozygous for a frameshift mutation in the POMC gene (6922InsC) that impairs the production of all melanocortin peptides, and that is associated with novel clinical features. Repeated clinical investigations from birth to age 18 yr are presented. Result: ACTH deficiency was diagnosed at birth. Hyperphagia and obesity became apparent before 2 yr of age and rapidly progressed [body mass index (BMI) Z-score, +7 SD at 2 yr, +9.7 SD at 13 yr; BMI, 50 kg/m2 at 18 yr). At puberty, the patient developed alterations in the somatotropic, gonadotropic, and thyroid axes necessitating hormonal replacement. Surprisingly, there were no obvious pigmentary features; neither the hair color nor measurements of skin reflectance distinguished between the patient and unaffected family members. However, chemical analysis of hair pigment revealed increased production of both pheomelanin and eumelanin. Conclusion: Molecular genetic abnormalities of POMC should always be considered in patients with early onset adrenal insufficiency and obesity, even in the presence of normal pigmentation and multiple pituitary hormone anomalies.

Original languageEnglish
Pages (from-to)4955-4962
Number of pages8
JournalJournal of Clinical Endocrinology and Metabolism
Volume93
Issue number12
DOIs
Publication statusPublished - Dec 2008

Fingerprint

Pro-Opiomelanocortin
Pigmentation
Young Adult
Genes
Mutation
Hair
Adrenocorticotropic Hormone
Skin
Body Mass Index
Obesity
Hair Color
Parturition
Melanocortins
Skin Pigmentation
Melanocyte-Stimulating Hormones
Adrenal Insufficiency
Hyperphagia
Peptides
Frameshift Mutation
Pituitary Hormones

ASJC Scopus subject areas

  • Biochemistry
  • Clinical Biochemistry
  • Endocrinology
  • Biochemistry, medical
  • Endocrinology, Diabetes and Metabolism

Cite this

Unexpected endocrine features and normal pigmentation in a young adult patient carrying a novel homozygous mutation in the POMC gene. / Clément, Karine; Dubern, Béatrice; Mencarelli, Monica; Czernichow, Paul; Ito, Shosuke; Wakamatsu, Kazumasa; Barsh, Gregory S.; Vaisse, Christian; Leger, Juliane.

In: Journal of Clinical Endocrinology and Metabolism, Vol. 93, No. 12, 12.2008, p. 4955-4962.

Research output: Contribution to journalArticle

Clément, Karine ; Dubern, Béatrice ; Mencarelli, Monica ; Czernichow, Paul ; Ito, Shosuke ; Wakamatsu, Kazumasa ; Barsh, Gregory S. ; Vaisse, Christian ; Leger, Juliane. / Unexpected endocrine features and normal pigmentation in a young adult patient carrying a novel homozygous mutation in the POMC gene. In: Journal of Clinical Endocrinology and Metabolism. 2008 ; Vol. 93, No. 12. pp. 4955-4962.
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