Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services

A teenage Afghan girl presented with seizure. Clinical features and laboratory investigations revealed elevated serum parathormone, high phosphate levels with low serum calcium. In third‐world countries, diagnosis of rare disorders, such as Albright hereditary osteodystrophy (AHO), can usually be de...

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Detalles Bibliográficos
Autores principales: Noor, Sahar, Hakimzada, Nasrin, Safi, Nijatullah, Alikozai, Sultan Mahmood, Rasooli, Abdul Jamil, Jalalzai, Tooryalai, Siddiqui, Qais, Sestani, Ahmad Jalil, Nasir, Najla, Noor, Sarah, Haidary, Ahmed Maseh, Khalid, Saifullah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842773/
https://www.ncbi.nlm.nih.gov/pubmed/36694647
http://dx.doi.org/10.1002/ccr3.6841

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842773/
https://www.ncbi.nlm.nih.gov/pubmed/36694647
http://dx.doi.org/10.1002/ccr3.6841

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