Usage of "hypophosphatemic ricket"

Disorder characterized by hypophosphatemi, rickets, osteomalacia, resulting from lack of phosphate reabsorption by the kidneys and possible defects in vitamin D metabolism.

Veure'n més

vitamin d-resistant osteomalacia

Termes relacionats

disease

Ús de hypophosphatemic ricket en anglès

X-linked hypophosphatemic rickets and autosomal dominant hypophosphatemic rickets are inherited phosphate wasting disorders. 
 Pubmed 

Human DMP1 mutations are responsible for the condition known as autosomal recessive hypophosphatemic rickets. 
 Pubmed 

A subset of those who survive eventually develop hypophosphatemic rickets. 
 Pubmed 

Skeletal muscle dysfunction accompanies the clinical disorders of chronic kidney disease (CKD) and hereditary hypophosphatemic rickets. 
 Pubmed 

X-linked hypophosphatemic rickets in humans is caused by mutations in the PEX gene which codes for a protein homologous to neutral endopeptidases. 
 Pubmed 

X-linked hypophosphatemic rickets results from mutations in the PHEX gene, which codes for a protein that is a member of the neutral endopeptidase family. 
 Pubmed 

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Significats de hypophosphatemic ricket en anglès