Vitamin D-Dependent Rickets Type 1B (25-Hydroxylase Deficiency): A Rare Condition or a Misdiagnosed Condition?

Author:

Molin Arnaud1234,Wiedemann Arnaud56,Demers Nick7,Kaufmann Martin7,Do Cao Jérémy56,Mainard Laurent68,Dousset Brigitte9,Journeau Pierre610,Abeguile Geneviève1,Coudray Nadia1,Mittre Hervé124,Richard Nicolas13,Weryha Georges611,Sorlin Arthur12,Jones Glenville7,Kottler Marie-Laure123,Feillet Francois5613

Affiliation:

1. CHU de Caen; Department of Genetics, Molecular Genetics Laboratory and Reference Center for Rare Diseases of Calcium and Phosphorus Metabolism; Caen France

2. Université Caen Normandie; Medical School; Caen France

3. BioTARGEN; Université Caen Normandie; Caen France

4. OeReCa; Université Caen Normandie; Caen France

5. CHU de Nancy; Department of Pediatrics and Reference Center for Rare Hereditary Diseases of Metabolism; Vandoeuvre-lès-Nancy France

6. Université de Lorraine; Medical School; Vandoeuvre-lès-Nancy France

7. Queen's University; Department of Biomedical and Molecular Sciences; Kingston Canada

8. CHU de Nancy; Department of Radiology; Vandoeuvre-lès-Nancy France

9. CHU de Nancy; Department of Biochemistry; Vandoeuvre-lès-Nancy France

10. CHU de Nancy; Department of Orthopedic Pediatric Surgery; Vandoeuvre-lès-Nancy France

11. CHU de Nancy; Department of Endocrinology; Vandoeuvre-lès-Nancy France

12. CHU de Nancy; Department of Genetics; Vandoeuvre-lès-Nancy France

13. INSERM; U954 Nutrition - génétique et exposition aux risques environnementaux; Vandoeuvre-lès-Nancy France

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

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