The Narrative of a Patient with Leptin Receptor Deficiency: Personalized Medicine for a Rare Genetic Obesity Disorder

Leptin receptor (LEPR) deficiency is a rare genetic disorder that affects the body’s ability to regulate appetite and weight. For patients and their families, the disorder seriously disrupts daily life; however, little is published about this impact. We here report the experiences of a 10.5-year-old...

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Detalles Bibliográficos
Autores principales: Welling, Mila S., Kleinendorst, Lotte, van Haelst, Mieke M., van den Akker, Erica L.T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601614/
https://www.ncbi.nlm.nih.gov/pubmed/37393902
http://dx.doi.org/10.1159/000531529

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601614/
https://www.ncbi.nlm.nih.gov/pubmed/37393902
http://dx.doi.org/10.1159/000531529

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