| Literature DB >> 32238367 |
Mallory L Downie1,2, Sergio C Lopez Garcia1,2, Robert Kleta1,2, Detlef Bockenhauer3,2.
Abstract
The kidney tubules provide homeostasis by maintaining the external milieu that is critical for proper cellular function. Without homeostasis, there would be no heartbeat, no muscle movement, no thought, sensation, or emotion. The task is achieved by an orchestra of proteins, directly or indirectly involved in the tubular transport of water and solutes. Inherited tubulopathies are characterized by impaired function of one or more of these specific transport molecules. The clinical consequences can range from isolated alterations in the concentration of specific solutes in blood or urine to serious and life-threatening disorders of homeostasis. In this review, we focus on genetic aspects of the tubulopathies and how genetic investigations and kidney physiology have crossfertilized each other and facilitated the identification of these disorders and their molecular basis. In turn, clinical investigations of genetically defined patients have shaped our understanding of kidney physiology.Entities:
Keywords: Bartter-s syndrome; Emotions; Genomics; Homeostasis; Kidney; Kidney Tubules; Sensation; Series; Urinary Tract Physiological Phenomena; Water; kidney; kidney tubule; magnesium wasting disorders; nephrogenic diabetes insipidus; renal tubular acidosis; tubulopathies
Mesh:
Year: 2020 PMID: 32238367 PMCID: PMC8092065 DOI: 10.2215/CJN.14481119
Source DB: PubMed Journal: Clin J Am Soc Nephrol ISSN: 1555-9041 Impact factor: 8.237