Juvenile Paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation

Medicine & Life Sciences

• Hyperostosis corticalis deformans juvenilis 100%
• Vitamin D Deficiency 58%
• Osteoprotegerin 47%
• Mutation 29%
• Pamidronate 20%
• Craniosynostoses 18%
• Vitamin D 13%
• Serum 10%
• Failure to Thrive 9%
• Calcinosis 9%
• 25-hydroxyvitamin D 8%
• Loss of Function Mutation 8%
• Bone Fractures 8%
• Blindness 7%
• Acceleration 7%
• Cysteine 6%
• Alkaline Phosphatase 6%
• Phosphates 6%
• Young Adult 5%
• Pneumonia 5%
• Parents 5%
• Ligands 5%
• Calcium 5%
• Bone and Bones 4%
• Blood Vessels 4%
• Pain 4%
• Therapeutics 3%
• Child 3%
• Genes 2%