The Association of Pseudohypoparathyroidism Type Ia with Chiari Malformation Type I: A Coincidence or a Common Link?

A 19-month-old boy was referred for progressive weight gain. His past medical history included congenital hypothyroidism and developmental delay. Physical examination revealed characteristics of Albright Hereditary Osteodystrophy, macrocephaly, and calcinosis cutis. He had hypocalcemia, hyperphospha...

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Detalles Bibliográficos
Autores principales: Kashani, Paria, Roy, Madan, Gillis, Linda, Ajani, Olufemi, Samaan, M. Constantine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039284/
https://www.ncbi.nlm.nih.gov/pubmed/27703483
http://dx.doi.org/10.1155/2016/7645938

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039284/
https://www.ncbi.nlm.nih.gov/pubmed/27703483
http://dx.doi.org/10.1155/2016/7645938

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