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Setmelanotide: a promising advancement for pediatric patients with rare forms of genetic obesity

Examine Setmelanotide use in patients with rare genetic variants that disrupt the melanocortin pathway. RECENT FINDINGS: Between February 2017 and September 2018, 10 participants with pro-opiomelanocortin (POMC)/ proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency and 11 participants wi...

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Detalles Bibliográficos
Autores principales:	Trapp, Christine M., Censani, Marisa
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2023
Materias:	Special Commentaries
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9973437/ https://www.ncbi.nlm.nih.gov/pubmed/36722447 http://dx.doi.org/10.1097/MED.0000000000000798

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