X-linked Hypophosphatemic Rickets: Awareness, Knowledge, and Practice of Pediatric Endocrinologists in Arab Countries.

ASPED FGF-23 X-linked hypophosphatemic rickets burosomab

Journal

Journal of pediatric genetics
ISSN: 2146-4596
Titre abrégé: J Pediatr Genet
Pays: Germany
ID NLM: 101589859

Informations de publication

Date de publication:
Jun 2022
Historique:
received: 16 08 2020
accepted: 25 10 2020
entrez: 30 6 2022
pubmed: 15 12 2020
medline: 15 12 2020
Statut: epublish

Résumé

X-linked hypophosphatemic rickets (XLHR) is a genetic disease caused by inactivating pathogenic variants in

Identifiants

pubmed: 35769954
doi: 10.1055/s-0040-1721400
pii: 2000133
pmc: PMC9236740
doi:

Types de publication

Journal Article

Langues

eng

Pagination

126-131

Informations de copyright

Thieme. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of Interest None declared.

Références

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Auteurs

Asma Deeb (A)

Department of Pediatric Endocrinology, Sheikh Shakhbout Medical City, Abu Dhabi, United Arab Emirates.

Fahad Al Juraibah (FA)

Department of Pediatrics, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
Department of Pediatrics, College of Medicine, King Saud bin Abdulaziz University for Health Science, Riyadh, Saudi Arabia.

Muhammad Al Dubayee (MA)

Department of Pediatrics, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
Department of Pediatrics, College of Medicine, King Saud bin Abdulaziz University for Health Science, Riyadh, Saudi Arabia.

Abdelhadi Habeb (A)

Department of Pediatrics, Ministry of National Guard Health Affairs, Madinah, Saudi Arabia.

Classifications MeSH