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

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

Abstract 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 usua...

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Bibliographic Details
Main Authors: Sahar Noor, Nasrin Hakimzada, Nijatullah Safi, Sultan Mahmood Alikozai, Abdul Jamil Rasooli, Tooryalai Jalalzai, Qais Siddiqui, Ahmad Jalil Sestani, Najla Nasir, Sarah Noor, Ahmed Maseh Haidary, Saifullah Khalid
Format: Article
Language:English
Published: Wiley 2023-01-01
Series:Clinical Case Reports
Subjects:
Albright hereditary osteodystrophy
brachydactyly
hypocalcaemia
pseudohypoparathyrodism
Online Access:https://doi.org/10.1002/ccr3.6841

Internet

https://doi.org/10.1002/ccr3.6841

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