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Genetic causes of hypophosphatemia.
- Source :
-
Minerva medica [Minerva Med] 2024 Jun; Vol. 115 (3), pp. 320-336. Date of Electronic Publication: 2024 May 09. - Publication Year :
- 2024
-
Abstract
- Phosphate is a key component of mineralized tissues and is also part of many organic compounds. Phosphorus homeostasis depends especially upon intestinal absorption, and renal excretion, which are regulated by various hormones, such as PTH, 1,25-dihydroxyvitamin D, and fibroblast growth factor 23. In this review we provide an update of several genetic disorders that affect phosphate transporters through cell membranes or the phosphate-regulating hormones, and, consequently, result in hypophosphatemia.
- Subjects :
- Humans
Phosphates metabolism
Vitamin D metabolism
Vitamin D analogs & derivatives
Klotho Proteins
Phosphate Transport Proteins genetics
Phosphate Transport Proteins metabolism
PHEX Phosphate Regulating Neutral Endopeptidase genetics
Intestinal Absorption genetics
Glucuronidase genetics
Glucuronidase metabolism
Phosphorus metabolism
Hypophosphatemia genetics
Hypophosphatemia etiology
Fibroblast Growth Factor-23
Fibroblast Growth Factors metabolism
Fibroblast Growth Factors genetics
Parathyroid Hormone metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1827-1669
- Volume :
- 115
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Minerva medica
- Publication Type :
- Academic Journal
- Accession number :
- 38727708
- Full Text :
- https://doi.org/10.23736/S0026-4806.24.09198-5