or Autosomal Recessive Hypophosphatemic Rickets Type 2 (ARHR2), representing age-dependent phenotypes that evolve on a continuum over a lifetime. Of the 84 individuals with ENPP1 Deficiency in the ...

Children with this condition typically develop autosomal-recessive hypophosphatemic rickets type 2 (ARHR2), while adolescents and adults may develop osteomalacia, or softened bones. ARHR2 and ...

A high Tm Pi in hypophosphatemia is indicative of increased renal excretion secondary to a PTH-mediated mechanism, Fanconi syndrome, XLH, autosomal dominant hypophosphatemic rickets or oncogenic ...

ENPP1 Deficiency frequently manifests as Generalized Arterial Calcification of Infancy (GACI) or Autosomal Recessive Hypophosphatemic Rickets Type 2 (ARHR2), representing age-dependent phenotypes that ...

After genetic testing was carried out, it was found that the patient had a monoallelic inactivation mutations in the ENPP1 gene, which is the pathogenic gene of Autosomal-Recessive Hypophosphatemic ...

Following the establishment of an FGF23-related hypophosphatemic rickets and osteomalacia registry at KFSHRC and loss of follow-up of 12 family members who previously attended the hospital due to poor ...

A pharmacist has issued a warning that common medications could be contributing to a resurgence in Victorian diseases such as scurvy, shingles and rickets. Millions of Britons take prescription ...

Reluctantly, the couple signed over their parental rights. Alandria said she found the possibility of infantile rickets on her cell phone's search engine. Their rights were still revoked.

A science museum in the city looks back at the history of feeding children in schools and reminds us how fraught the efforts have been for more than 100 years. By Shannon Eblen Reporting from ...