Rabson-Mendenhall syndrome presented as severe acanthosis nigricans in an infant harboring novel mutations in the INSR gene: a case report

BackgroundRabson-Mendenhall Syndrome (RMS), a rare hereditary form of insulin resistance, is marked by severe hyperinsulinemia and early-onset acanthosis nigricans (AN) during childhood.Case presentationA case of a 15-month-old girl was reported, presenting with widespread acanthosis nigricans, grow...

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Hlavní autoři:	Shi Yan, Yu Sheng, Hai-zhen Hui, Chun-yan Zhou, De-ming Liu
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Frontiers Media S.A. 2025-04-01
Edice:	Frontiers in Pediatrics
Témata:	INSR gene Rabson-Mendenhall syndrome acanthosis nigricans case report acanthosis nigricans (AN)
On-line přístup:	https://www.frontiersin.org/articles/10.3389/fped.2025.1511429/full
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