X-linked hypophosphataemic rickets in children: clinical phenotype, therapeutic strategies, and molecular background.
Aleksandra RojekAleksandra RojekZofia KolesinskaDorota JurkiewiczKrystyna H ChrzanowskaMarek NiedzielaPublished in: Endokrynologia Polska (2020)
We report 3 novel mutations in the PHEX responsible for HR. Additionally, this study reports the effects of rhGH therapy for growth promotion in HR.
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