GENESIS Pharma’s Post

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23 October, On this #InternationalXLHAwarenessDay, join us in raising awareness of X-linked hypophosphatemia #XLH. XLH is a rare metabolic bone disease, typically presenting in early childhood. It is the most common form of hereditary rickets. Early detection within the entire family and consistency to therapy can have a profound benefit to patients.

Antonis Louroutziatis

Country Lead Hema-Onco, I&I and Specialty Unit at Genesis Pharma Cyprus

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