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Monogenic Non-Syndromic Obesity

MedGen UID:
893427
•Concept ID:
CN239457
•
Disease or Syndrome

Recent clinical studies

Etiology

Sequencing methods, functional characterization, prevalence, and penetrance of rare coding mutations in panels of monogenic obesity genes from the leptin-melanocortin pathway: A systematic review.
Dosda S, Renard E, Meyre D
Obes Rev 2024 Aug;25(8):e13754. Epub 2024 May 23 doi: 10.1111/obr.13754. PMID: 38779716
The Spectrum of Genetic Variants Associated with the Development of Monogenic Obesity in Qatar.
AbouHashem N, Zaied RE, Al-Shafai K, Nofal M, Syed N, Al-Shafai M
Obes Facts 2022;15(3):357-365. Epub 2022 Jan 13 doi: 10.1159/000521851. PMID: 35026759Free PMC Article

Prognosis

The Spectrum of Genetic Variants Associated with the Development of Monogenic Obesity in Qatar.
AbouHashem N, Zaied RE, Al-Shafai K, Nofal M, Syed N, Al-Shafai M
Obes Facts 2022;15(3):357-365. Epub 2022 Jan 13 doi: 10.1159/000521851. PMID: 35026759Free PMC Article

Clinical prediction guides

The Spectrum of Genetic Variants Associated with the Development of Monogenic Obesity in Qatar.
AbouHashem N, Zaied RE, Al-Shafai K, Nofal M, Syed N, Al-Shafai M
Obes Facts 2022;15(3):357-365. Epub 2022 Jan 13 doi: 10.1159/000521851. PMID: 35026759Free PMC Article

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    • ClinVar
      Related medical variations
    • PMC Articles
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    • PubMed
      Related literature resources in PubMed

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