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Significados de hypophosphatemic vitamin d-resistant rickets em inglês

Human disease.

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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