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Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services
- Source :
- Clinical Case Reports, Vol 11, Iss 1, Pp n/a-n/a (2023)
- Publication Year :
- 2023
- Publisher :
- Wiley, 2023.
-
Abstract
- 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 thirdâworld countries, diagnosis of rare disorders, such as Albright hereditary osteodystrophy (AHO), can usually be delayed due to scarcity of standard medical and diagnostic services.
Details
- Language :
- English
- ISSN :
- 20500904
- Volume :
- 11
- Issue :
- 1
- Database :
- Directory of Open Access Journals
- Journal :
- Clinical Case Reports
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.981cd91845b645da91ea791e88fdb96e
- Document Type :
- article
- Full Text :
- https://doi.org/10.1002/ccr3.6841