Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function VDR mutation

Journal article

Peer reviewed

Muhammad Faiyaz-Ul-Haque, Waheeb AlDhalaan, Abdullah AlAshwal, Bassam S. Bin-Abbas, Afaf AlSagheir, Maram Alotaiby, Zulqurnain Rafiq and Syed H.E. Zaidi

Journal of Pediatric Endocrinology and Metabolism, Vol.31(8), pp.861-868

28/08/2018

PMID: 29949513

Abstract

alopecia

growth retardation

hereditary 1,25-dihydroxyvitamin D-resistant rickets

treatment

vitamin D receptor mutation

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Title: Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function VDR mutation
Creators - without role: Muhammad Faiyaz-Ul-Haque - King Khalid University Hospital
Waheeb AlDhalaan - King Faisal Specialist Hospital & Research Centre
Abdullah AlAshwal - Department of Pediatrics – MBC 58, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
Bassam S. Bin-Abbas - King Faisal Specialist Hospital & Research Centre
Afaf AlSagheir - King Faisal Specialist Hospital & Research Centre
Maram Alotaiby - King Saud University
Zulqurnain Rafiq - King Saud University
Syed H.E. Zaidi - Ontario Institute for Cancer Research
Publication Details: Journal of Pediatric Endocrinology and Metabolism, Vol.31(8), pp.861-868
Publisher: De Gruyter
Number of pages: 8
Identifiers: 9949431208331
Academic Unit: King Saud University
Language: English
Resource Type: Journal article