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Significats de phosphopenic rickets en anglès

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

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      Examples for "acquired vitamin d resistant rickets"
      Examples for "acquired vitamin d resistant rickets"
      1
      X-linked hypophosphatemic rickets and autosomal dominant hypophosphatemic rickets are inherited phosphate wasting disorders.
      Pubmed
      2
      Human DMP1 mutations are responsible for the condition known as autosomal recessive hypophosphatemic rickets.
      Pubmed
      3
      A subset of those who survive eventually develop hypophosphatemic rickets.
      Pubmed
      4
      Skeletal muscle dysfunction accompanies the clinical disorders of chronic kidney disease (CKD) and hereditary hypophosphatemic rickets.
      Pubmed
      5
      X-linked hypophosphatemic rickets in humans is caused by mutations in the PEX gene which codes for a protein homologous to neutral endopeptidases.
      Pubmed
      1
      X-linked hypophosphatemic rickets and autosomal dominant hypophosphatemic rickets are inherited phosphate wasting disorders.
      Pubmed
      2
      Human DMP1 mutations are responsible for the condition known as autosomal recessive hypophosphatemic rickets.
      Pubmed
      3
      A subset of those who survive eventually develop hypophosphatemic rickets.
      Pubmed
      4
      Skeletal muscle dysfunction accompanies the clinical disorders of chronic kidney disease (CKD) and hereditary hypophosphatemic rickets.
      Pubmed
      5
      X-linked hypophosphatemic rickets in humans is caused by mutations in the PEX gene which codes for a protein homologous to neutral endopeptidases.
      Pubmed