Novel homozygous leptin receptor mutation in an infant with monogenic obesity

Monogenic obesity can be caused by a mutation in one of the single genes involved in hunger and satiety. The most common mutations affect melanocortin 4 (MC4) followed by the leptin gene and its receptor. Leptin receptor (LEPR) gene mutation is an extremely rare endocrine disease characterized by ea...

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Detalles Bibliográficos
Autores principales: Boro, Hiya, Bundela, Vikash, Mannar, Velmurugan, Nagendra, Lakshmi, Jain, Vinita, Jain, Bimal, Kumar, Senthil, Agstam, Sourabh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2023
Materias:
Case report | Opis przypadku
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10411088/
https://www.ncbi.nlm.nih.gov/pubmed/37728464
http://dx.doi.org/10.5114/pedm.2023.129344

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10411088/
https://www.ncbi.nlm.nih.gov/pubmed/37728464
http://dx.doi.org/10.5114/pedm.2023.129344

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