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Evaluation of Methods That Estimate Glomerular Filtration Rate in Patients With Prader-Willi Syndrome

Background: Prader-Willi syndrome (PWS) is a rare, complex, multisystem disorder caused by the loss of multiple paternally expressed genes on chromosome 15q11-13 and is present in 1/15,000-30,000 individuals. Characteristics of PWS include low muscle mass and hypotonia, accumulation of excess body f...

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Detalles Bibliográficos
Autores principales:	Ko, Paul Jihoon, Ballal, Shaila, Hirano, Patricia, Cowen, Neil
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2021
Materias:	Pediatric Endocrinology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8089497/ http://dx.doi.org/10.1210/jendso/bvab048.1452

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