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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...
| Autores principales: | , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2023
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| Materias: | |
| 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 |
| _version_ | 1784870220459933696 |
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| author | 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 |
| author_facet | 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 |
| author_sort | Noor, Sahar |
| collection | PubMed |
| description | 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 delayed due to scarcity of standard medical and diagnostic services. |
| format | Online Article Text |
| id | pubmed-9842773 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2023 |
| publisher | John Wiley and Sons Inc. |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-98427732023-01-23 Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services 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 Clin Case Rep Case Report 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 delayed due to scarcity of standard medical and diagnostic services. John Wiley and Sons Inc. 2023-01-16 /pmc/articles/PMC9842773/ /pubmed/36694647 http://dx.doi.org/10.1002/ccr3.6841 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
| spellingShingle | Case Report 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 Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services |
| title | Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services |
| title_full | Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services |
| title_fullStr | Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services |
| title_full_unstemmed | Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services |
| title_short | Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services |
| title_sort | albright hereditary osteodystrophy: delay in the diagnosis of a rare disorder due to restricted medical services |
| topic | Case Report |
| url | 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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