Co-occurrence of two rare diseases: a child with phenylketonuria and WNT1 osteoporosis

pubmed: wnt1 2024-12-21

Summary:

CONCLUSION: In a patient with a chronic disorder known to affect the skeleton, the presence of disproportionally severe osteoporosis should prompt further diagnostic work up, in order to explain the severe bone phenotype, thus enabling more efficient and targeted therapeutic interventions.

Link:

https://pubmed.ncbi.nlm.nih.gov/39602902/?utm_source=Other&utm_medium=rss&utm_campaign=None&utm_content=16uwQpOeqFYN8R4TKOtwPy2utpqy9ex2oldalD2yF_fQHv2caq&fc=None&ff=20241221000752&v=2.18.0.post9+e462414

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Exome » pubmed: wnt1

Tags:

Authors:

Artemis Doulgeraki, Fan Wang, Anastasia Skouma, Eleana Petropoulou, Symeon Tournis, Alice Costantini, Outi Mäkitie

Date tagged:

12/21/2024, 00:07

Date published:

11/27/2024, 06:00