Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services-Reference-Cited by-同舟云学术

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

Published:2023-01 Issue:1 Volume:11 Page:
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clinical Case Reports

Author:

Noor Sahar¹,Hakimzada Nasrin¹,Safi Nijatullah¹,Alikozai Sultan Mahmood¹,Rasooli Abdul Jamil¹,Jalalzai Tooryalai¹,Siddiqui Qais¹,Sestani Ahmad Jalil¹,Nasir Najla²,Noor Sarah³^ORCID,Haidary Ahmed Maseh⁴^ORCID,Khalid Saifullah⁵

Affiliation:

1. Department of Paediatric Medicine French Medical Institute for Mothers and Children (FMIC) Kabul Kabul Afghanistan

2. Department of Medicine Rabia Balkhi Hospital Kabul Afghanistan

3. Department of Oncology Ali Abad Hospital Kabul Afghanistan

4. Department of Pathology French Medical Institute for Mothers and Children (FMIC) Kabul Kabul Afghanistan

5. Department of Radiology Jumhoriat Hospital Kabul Afghanistan

Abstract

AbstractA 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.

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.6841

Reference14 articles.

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2. Albright Hereditary Osteodystrophy, Pseudohypoparathyroidism, and Gs Deficiency

3. Pseudohypoparathyroidism‐an Example of ‘Seabright‐Bantam syndrome’;Albright F;Endocrinolog,1942

4. Pseudo‐pseudohypoparathyroidism;Albright F;Trans Assoc Am Physicians,1952

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