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RF12 | PSUN125 Lymphoma in Congenital Leptin Deficiency: Comorbidity or Adverse Effect?

BACKGROUND: Congenital leptin deficiency (CLD) is a rare autosomal recessive form of monogenic obesity caused by loss-of-function mutations in the leptin gene. Targeted therapy is available in the form of recombinant human leptin (metreleptin). We previously reported baseline characteristics of one...

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Detalles Bibliográficos
Autores principales:	Torchen, Laura, Hakamy, Beth, Gordon, Leo I, Yaseen, Nabeel R, Neff, Lisa M
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2022
Materias:	Adipose Tissue, Appetite, & Obesity
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624871/ http://dx.doi.org/10.1210/jendso/bvac150.065

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