Rabson-Mendenhall Syndrome

Rabson-Mendenhall syndrome (RMS) is a rare genetic disorder characterized by growth retardation, dysmorphisms, lack of subcutaneous fat, acanthosis nigricans, enlarged genitalia, hirsutism, dysplastic dentition, coarse facial features, abnormal glucose homeostasis, hyperinsulinemia and pineal hyperp...

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Detalles Bibliográficos
Autores principales: Hassan, Iffat, Altaf, Hinah, Yaseen, Atiya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
E-IJD Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248531/
https://www.ncbi.nlm.nih.gov/pubmed/25484423
http://dx.doi.org/10.4103/0019-5154.143579

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248531/
https://www.ncbi.nlm.nih.gov/pubmed/25484423
http://dx.doi.org/10.4103/0019-5154.143579

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