An intricate case of sporadic pseudohypoparathyroidism type 1B with a review of literature

Pseudohypoparathyroidism comprehends an assorted group of genetically rare disorders that share end-organ resistance to parathyroid hormone. Genetic and epigenetic modifications on guanine nucleotide-binding protein alpha-stimulating gene locus are the most common underlying mechanisms associated wi...

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Detalles Bibliográficos
Autores principales: Silva, José Diogo Ramalho e, da Rocha, Gustavo Filipe Melo Alves, Oliveira, Maria João Martins
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Endocrinologia e Metabologia 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10528691/
https://www.ncbi.nlm.nih.gov/pubmed/33320452
http://dx.doi.org/10.20945/2359-3997000000316

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10528691/
https://www.ncbi.nlm.nih.gov/pubmed/33320452
http://dx.doi.org/10.20945/2359-3997000000316

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