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Mohamed Kenaway

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Review Open access Aug 2026

Phenotypic spectrum and quality of life in pediatric Bruck syndrome due to FKBP10 and PLOD2 variants: a 2-center United Arab Emirates experience

Abstract Bruck syndrome is a rare autosomal recessive form of OI caused by biallelic variants in FKBP10 or PLOD2, and characterized by fragility fractures with congenital or progressive joint contractures. We describe 13 patients from 2 tertiary pediatric centers in the United Arab Emirates and report exploratory healt...

M. Awad, Rania Eladl, A. Abdalla et al. · 0 citations

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