A clinical follow-up of 35 Brazilian patients with Prader-Willi Syndrome

OBJECTIVE: Prader-Willi Syndrome is a common etiology of syndromic obesity that is typically caused by either a paternal microdeletion of a region in chromosome 15 (microdeletions) or a maternal uniparental disomy of this chromosome. The purpose of this study was to describe the most significant cli...

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Detalles Bibliográficos
Autores principales: Quaio, Caio Robledo D'Angioli Costa, de Almeida, Tatiana Ferreira, Albano, Lilian Maria José, Gomy, Israel, Bertola, Debora Romeo, Varela, Monica Castro, Koiffmann, Celia P, Kim, Chong Ae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2012
Materias:
Clinical Science
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3416898/
https://www.ncbi.nlm.nih.gov/pubmed/22948460
http://dx.doi.org/10.6061/clinics/2012(08)11

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3416898/
https://www.ncbi.nlm.nih.gov/pubmed/22948460
http://dx.doi.org/10.6061/clinics/2012(08)11

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