Hereditary kidney diseases associated with hypomagnesemia

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis types 1 and 2

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is a rare autosomal recessive tubular disorder characterized by excessive urinary loss of Mg²⁺ and Ca²⁺, bilateral nephrocalcinosis, and progressive chronic kidney disease (CKD) [17]. FHHNC patients typically present during early childhood or before adolescence with recurrent urinary tract infections, polyuria, polydipsia, nephrolithiasis, and failure to thrive [18–21]. FHHNC patients may show a pronounced decline in glomerular filtration rate at the time of diagnosis, and approximately one-third of cases progress to chronic renal failure during childhood or adolescence [21,22]. In contrast to patients with other hypomagnesemias, FHHNC patients have high serum levels of parathyroid hormone (PTH) before the onset of chronic renal failure [1,19,23]. In some cases, patients present amelogenesis imperfecta [24,25]. Clinical signs of severe hypomagnesemia such as seizures and muscular tetany are rare.

FHHNC is caused by recessive mutations in CLDN16 (FHHNC type 1, OMIM #248250) or CLDN19 (FHHNC type 2, OMIM #248190) [3,4]. Patients with mutations in CLDN19 also present ocular abnormalities such as severe myopia, nystagmus, and macular colobamata [4,21,26]. CLDN16 and CLDN19 encode the tight junction proteins claudin-16 and claudin-19, respectively, which are strongly expressed in the kidney [3,4]. Claudin-19 is also expressed in peripheral neurons and retina [4,27]. Claudin-16 and claudin-19 form heteromeric paracellular cation channels in the TAL that regulate Ca²⁺ and Mg²⁺ transport [28,29]. The reabsorption of Mg²⁺ is greatly dependent on the transepithelial potential as a driving force, which is created by a transepithelial NaCl concentration gradient. CLDN16 and CLDN19 mutations have been shown to impair the permeating function of these channels, resulting in a reduced lumen-positive potential and the simultaneous loss of the driving force for Mg²⁺ reabsorption [22,28].

Hypomagnesemia with secondary hypocalcemia

Hypomagnesemia with secondary hypocalcemia (HSH, OMIM #602014) is a rare autosomal recessive disorder characterized by severe hypomagnesemia associated with hypocalcemia. The levels of serum Mg²⁺ in patients with HSH are usually much lower than in patients with other types of hereditary hypomagnesemias [30]. The disease usually presents in early infancy, with neurological symptoms including tetany and severe seizures that are refractory to anticonvulsant therapy [30,31]. HSH patients have very low serum levels of PTH. Persistent low levels of serum Mg²⁺ likely cause secondary hypocalcemia by inhibiting PTH secretion and inducing resistance at the receptor sites [30]. The main defect in HSH is a reduction in intestinal Mg²⁺ absorption, which is in contrast to all other identified hereditary hypomagnesemias, along with reduced Mg²⁺ reabsorption in the DCT with renal Mg²⁺ wasting [31,32].

HSH is caused by recessive loss-of-function mutations in the TRPM6 gene, which encodes the TRPM6 cation channel [31,32]. TRPM6 is predominantly expressed in the apical membrane of the intestinal and renal DCT epithelial cells, where it is involved in Mg²⁺ reabsorption [7]. Its channel activity and expression are regulated by several factors including EGF and adenosine triphosphate (ATP) [14]. TRPM6 mutations identified in HSH patients disrupt Mg²⁺ conductance through the channel, both in the colon and DCT, causing hypomagnesemia [7]. However, the mechanisms leading to this disease are not entirely known. TRPM6 interacts with its close homolog TRPM7 to form functional heteromeric TRPM6/TRPM7 Mg²⁺ channels [8]. TRPM6 and TRPM7 contain a transmembrane ion channel segment covalently joined to a cytosolic serine/threonine protein kinase domain at the carboxy terminus. The kinase domain is cleaved from the channel segment and, after its translocation to the nucleus, it regulates the transcription of many genes involved in development [33]. Therefore, it has been suggested that TRPM6 may play a much wider role in the cell than only in Mg²⁺ homeostasis [33].

Isolated recessive hypomagnesemia

Isolated recessive renal hypomagnesemia is a rare disorder characterized by hypomagnesemia and normocalciuria [34]. Hypomagnesemia is due to renal Mg²⁺ wasting. Patients show seizures and neurodevelopmental delay during childhood. Only two affected girls from a consanguineous family have been reported, and no other biochemical abnormalities were identified in these patients. A homozygous missense mutation in the EGF gene coding for pro-EGF was identified as the underlying genetic defect [34]. Pro-EGF is a type I membrane-bound precursor protein that is proteolytically cleaved to generate the soluble EGF peptide hormone. EGF binds with high affinity to the renal epidermal growth factor receptor (EGFR) at the basolateral membrane of the DCT. EGFR activation triggers a signaling cascade leading to an increase of TRPM6 channels on the apical membrane and increased Mg²⁺ reabsorption [14]. The disease-causing EGF mutation results in diminished sorting of pro-EGF, preventing adequate secretion of the EGF hormone [34]. This leads to inadequate stimulation of the EGFR, and therefore insufficient activation of the TRPM6 channel, which results in reduced reabsorption of Mg²⁺.

Neonatal inflammatory skin and bowel disease type 2

Using whole-exome sequencing, a rare homozygous missense mutation (p.Gly428Asp) in EGFR was identified in a child with an inflammatory syndrome affecting the skin, bowel, and lungs (OMIM #616069) [35]. The pregnancy was complicated by polyhydramnios and the child was born prematurely. Laboratory tests revealed low serum levels of magnesium. The child showed failure to thrive and died at 2.5 years of age from widespread cutaneous and pulmonary infections in addition to electrolyte imbalance. Results of a skin biopsy and immunofluorescence microscopy studies revealed that the mutation p.Gly428Asp reduces EGFR plasma membrane localization [35].

Hypomagnesemia, seizures, and mental retardation disorder type 1

Hypomagnesemia, seizures, and mental retardation disorder (HSMR) type 1 is a complex rare condition characterized by renal Mg²⁺ loss that results in hypomagnesemia, infantile or juvenile epileptic seizures, and intellectual disability [36,37]. Patients also show autistic features, aggressive behavior, variable degrees of delayed psychomotor development, speech limitations, impaired motor skills, and in some cases obesity [37,38]. HSMR type 1 is caused by loss-of-function mutations in the CNNM2 gene, which encodes the transmembrane protein CNNM2 [36–38]. Most HSMR type 1 patients carry heterozygous mutations that are generated de novo or inherited in an autosomal dominant pattern (OMIM #616418) [36–38]. However, a recessive mode of inheritance has been reported for several families [37,39]. Patients with recessive CNNM2 mutations show a severe phenotype, including brain malformations, refractory epilepsy, and acute intellectual disability (OMIM #613882).

CNNM2 is expressed in many organs and tissues including brain and kidney. In the kidney, CNNM2 is predominantly expressed at the basolateral membrane of the DCT cells, where it is associated with Mg²⁺ reabsorption [36,40]. Whether CNNM2 is itself an Mg²⁺ transporter or a regulator of Mg²⁺ transport is unclear [11]. However, CNNM2 pathogenic mutations reduce its expression in the plasma membrane, resulting in defective Mg²⁺ reabsorption and Mg²⁺ wasting [11,38]. Furthermore, recent studies revealed that Mg²⁺-ATP binding to the intracellular C-terminus of CNNM2 is required for protein dimerization and Mg²⁺ efflux [41]. Disease-causing mutations that are located in the Mg²⁺-ATP-binding site abolish ATP binding and Mg²⁺ efflux activity. The basis of the neurological defects remains unknown.

Bartter syndrome type 3

Bartter syndrome (BS) includes a group of several tubulopathies characterized by renal salt wasting, hypokalemia, hypochloremic metabolic alkalosis, hyperreninemia, hyperaldosteronism, and low to normal blood pressure [42,43]. Patients usually present during the first years of life with failure to thrive, polyuria, and polydipsia. The main pathogenic mechanism in these tubulopathies is defective salt reabsorption predominantly in the TAL. Five different types of BS have been identified based on the gene involved [43]. Patients with BS type 3 or classic BS (OMIM #607364) develop hypomagnesemia during childhood or later in life [44]. This disorder is characterized by a great clinical variability, and there is a correlation between the severity of mutations and younger age at diagnosis [44,45].

BS type 3 is caused by recessive loss-of-function mutations of the CLCNKB gene, which encodes the kidney-specific Cl^– channel ClC-Kb that is involved in NaCl reabsorption in the renal tubule [6]. The ClC-Kb protein is expressed in the basolateral membrane of epithelial cells in the TAL and the DCT. In these tubular segments, Cl^– exits the cell through ClC-Ka and ClC-Kb channels. Mutations in CLCNKB alter the intracellular Cl^– regulation, which subsequently interferes with the generation of the lumen-positive potential and results in salt wasting and possibly hypomagnesemia.

Gitelman syndrome

Gitelman syndrome (GS, OMIM #263800) is an autosomal recessive salt-losing tubulopathy characterized by hypokalemic metabolic alkalosis, low or normal blood pressure, hypocalciuria, and hypomagnesemia with renal Mg²⁺ wasting [46]. GS is the most common cause of hereditary hypomagnesemia and is usually detected during adolescence or adulthood. GS may be asymptomatic or associated with mild symptoms including chronic fatigue, muscle weakness, thirst, salt craving, nocturia, and cramps, which can considerably reduce the quality of life [47]. Severe complications such as cardiac arrhythmias have been reported in some cases [46].

GS is caused by recessive inactivating mutations of the SLC12A3 gene encoding the thiazide-sensitive NCC, which is localized in the apical membrane of DCT cells, where it plays a fundamental role in the reabsorption of Na⁺ and Cl^– [48,49]. NCC mutations lead to reduced reabsorption, which results in Na⁺ and Cl^– wasting, hypovolemia, and subsequent hyperaldosteronism with metabolic alkalosis [50]. The pathogenesis of hypocalciuria and hypomagnesemia may be explained by the compensatory paracellular reabsorption of Na⁺ and Ca²⁺ in the PT due to volume reduction and by decreased apical expression of TRPM6 [51]. There is phenotypic variability in GS, including in patients with the same SLC12A3 mutation.

Autosomal dominant hypocalcemia with hypercalciuria

Autosomal dominant hypocalcemia with hypercalciuria (ADHH, OMIM #601198) is a rare disorder of calcium homeostasis characterized by variable levels of hypocalcemia and low or normal serum levels of PTH [52]. Patients also present with hypomagnesemia, hypermagnesuria, hyperphosphatemia, and hypercalciuria [52,53]. Hypocalcemia is a derived effect of hypomagnesemia as a result of parathyroid failure or PTH resistance [30]. ADHH patients may develop hypocalcemic symptoms (paresthesias, carpopedal spasm, and seizures), and some have renal and basal ganglia calcifications, but others are asymptomatic [52].

ADHH is caused by heterozygous gain-of-function mutations in the CASR gene [52,54]. This gene encodes the extracellular CaSR, a G protein-coupled receptor that is highly expressed in parathyroid glands and kidneys [53]. In the kidney, CaSR is highly expressed in the basolateral membrane of the TAL, where it regulates Ca²⁺ reabsorption independently of PTH [53,55]. A signaling pathway including two microRNAs and the tight junction proteins claudin-14 and claudin-16 mediates the effect of CaSR on renal Ca²⁺ and Mg²⁺ excretion [5]. Activating mutations of CaSR increase the expression of claudin-14, which binds to claudin-16 and blocks the cation permeability of the claudin-16/claudin-19 channel.

Episodic ataxia type 1

Loss-of-function mutations in the KCNA1 gene are typically associated with an autosomal dominant neurological disorder called episodic ataxia type 1 (EA1, OMIM #160120), which is characterized by recurring episodes of ataxia and myokymia from early childhood [13]. The clinical phenotype in EA1 patients can include seizures, epilepsy, and, in some cases, paroxysmal kinesigenic dyskinesia, cataplexy, myokymia, and hypomagnesemia [56]. These symptoms can appear alone or in combination with EA1. A genotype-phenotype correlation analysis in a large cohort of EA1 patients revealed high inter- and intrafamilial variability of symptoms, but the penetrance of hypomagnesemia has not been evaluated [57].

The KCNA1 gene encodes the α subunit of the voltage-gated potassium channel Kv1.1, which is abundantly expressed in specific neurons and plays an important role in regulating neuronal excitability in the central and peripheral nervous system [57]. In the kidney, KCNA1 is exclusively expressed at the apical membrane of the DCT cells alongside the Mg²⁺ transporter TRPM6 [58]. Previous studies suggested that potassium (K⁺) secretion via Kv1.1 provides the electrochemical gradient needed for Mg²⁺ reabsorption by the TRPM6 channel [58,59]. Interestingly, two specific KCNA1 heterozygous mutations, p.Asn255Asp and p.Leu328Val, have been associated with hypomagnesemia, leading to muscle cramps and tetanic episodes [58,59]. Electrophysiological analyses showed that both amino acid substitutions result in nonfunctional Kv1.1 channels [58–60]. The reduction in the K⁺ conductance depolarizes the apical membrane of DCT cells, reducing the electrical driving force and leading to renal Mg²⁺ loss. The frequency of hypomagnesemia in patients with KCNA1 mutations may be greater than reported, since serum Mg²⁺ levels have not been examined in all EA1 patients. Additional research is needed to understand the association of KCNA1 mutations with hypomagnesemia.

Isolated dominant hypomagnesemia

Isolated dominant hypomagnesemia is a rare autosomal dominant disorder characterized by hypomagnesemia, hypocalciuria, and occasionally chondrocalcinosis (OMIM #154020) [61]. Some patients suffer from muscle cramps, episodes of convulsions, or chondrocalcinosis [61,62]. This disease has been identified in only three families who carry the same missense mutation, p.Gly41Arg, in the FXYD2 gene and appear to be descendants of a common ancestor [62,63]. FXYD2 encodes the kidney-specific regulatory γ-subunit of basolateral Na⁺, K⁺-ATPase, which is composed of a catalytic α subunit and an auxiliary β subunit. The Na⁺, K⁺-ATPase complex maintains the electrochemical gradients of Na⁺ and K⁺ across the basolateral plasma membrane that provide the driving force for transepithelial Mg²⁺ transport particularly in the DCT [15]. There are two splice variants of the γ-subunit: FXYD2a, which is expressed mainly in the TAL and PT, and FXYD2b, which is expressed exclusively in the basolateral membrane of the DCT and collecting duct [64]. Expression studies showed that the p.Gly41Arg mutation causes incorrect trafficking of the mutant γ FXYD2b subunit, preventing its interaction with the α and β Na⁺, K⁺-ATPase subunits [62]. This leads to destabilization and reduction of Na⁺, K⁺-ATPase activity in the DCT, which eventually results in decreased Mg²⁺ uptake and renal Mg²⁺ loss.

Hypomagnesemia, seizures, and mental retardation disorder type 2

Recently, three children from non-consanguineous families were reported who presented with generalized seizures in infancy associated with severe intellectual disability, massive renal Mg²⁺ wasting, and hypomagnesemia (HSMR type 2; OMIM #618314) [65]. Other findings included significant developmental delay and limited motor skills. Mutational analysis identified heterozygous de novo mutations in the ATP1A1 gene encoding the catalytic α1 subunit of the Na⁺, K⁺-ATPase [65]. This ubiquitously expressed subunit is the major α isoform in the kidney and is present in practically all cell types of the central nervous system [15]. Dominant and de novo mutations in ATP1A1 are also the cause of autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2) [66]. To the best of our knowledge, serum Mg²⁺ levels have not been studied in CMT2 patients. Functional studies of the mutant Na⁺, K⁺-ATPase α1 subunits revealed loss of pump activity and anomalous cation permeability, leading to membrane depolarization [65]. These discoveries emphasize the essential task of the catalytic α1 subunit of the Na⁺, K⁺-ATPase in renal tubular Mg²⁺ transport and neuronal activity. Since ATP1A1 is expressed in the TAL and DCT, it could affect transport in both tubular segments.

Epilepsy, ataxia, sensorineural deafness, and tubulopathy/seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance syndrome

Epilepsy, ataxia, sensorineural deafness, and tubulopathy (EAST) syndrome or seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME) syndrome (OMIM #612780) is an autosomal recessive disease characterized by early-onset epilepsy, delayed psychomotor development, ataxia, sensorineural deafness, and a salt-wasting tubulopathy with or without mental retardation [67,68]. The renal phenotype develops during the course of the disease and comprises polyuria, hypokalemia, metabolic alkalosis, hypocalciuria, and hypomagnesemia [69,70]. Plasma renin and aldosterone levels are increased and blood pressure is at the low end of the normal range. Urinary findings include K⁺, Mg²⁺, and Na⁺ wasting.

This complex disorder is caused by loss-of-function mutations in the KCNJ10 gene encoding Kir4.1, one of the components of the inwardly rectifying K⁺ channel Kir4.1/Kir5.1 [16,67,68]. KCNJ10 is mainly expressed in glial cells of the brain, the stria vascularis of the inner ear, and the kidney [69]. The renal phenotype of patients with EAST/SeSAME syndrome closely resembles that of patients with GS, suggesting that KCNJ10 mutations mainly impair transport in the DCT. In the kidney, Kir4.1 is expressed in the basolateral membrane of the DCT and is involved in K⁺ recycling, which is needed for the activity of Na⁺, K⁺-ATPase, and generation of a negative transmembrane potential [16]. Mutations that inactivate Kir4.1 function lead to a depolarization of the basolateral membrane and to a reduction of the driving force for anion channels and Na⁺-coupled exchangers. This alteration in membrane voltage could also affect other transport processes, such as those for Cl^– and Mg²⁺, which could explain the Mg²⁺ loss detected in patients with EAST/SeSAME syndrome.

Autosomal dominant tubulointerstitial kidney disease caused by HNF1B mutations

Autosomal dominant tubulointerstitial kidney disease (ADTKD) comprises a group of rare kidney disorders characterized by tubular damage and interstitial fibrosis without glomerular lesions [71]. Affected individuals usually develop CKD and end-stage renal disease in adulthood. Heterozygous mutations in several genes cause ADTKD, and this disease is subdivided into several subtypes based on the mutated gene [71].

ADTKD subtype HNF1B (ADTKD-HNF1B, OMIM #137920) is associated with hypomagnesemia [72,73]. The phenotypes detected in ADTKD-HNF1B patients are very heterogeneous and may appear during pregnancy, in childhood, or in adulthood [73]. Symptoms include renal cysts, kidney malformations, abnormalities of the genital tract and liver, and maturity-onset diabetes of the young (MODY) type 5 [72,74]. Hypomagnesemia and hypermagnesuria are observed in approximately 50% of patients [72,73].

ADTKD-HNF1B is caused by heterozygous mutations of the HNF1B gene, which encodes the developmentally regulated transcription factor hepatocyte nuclear factor-1β (HNF1β) [72,74,75]. These mutations are inherited in a dominant inheritance pattern or appear de novo. HNF1β regulates tissue-specific gene expression in epithelial cells of several organs, including the kidneys, pancreas, liver, and urogenital tract [76]. In the adult kidney, HNF1β is expressed in epithelial cells of all tubular segments. However, its role in renal Mg²⁺ reabsorption seems to take place in the DCT, since hypomagnesemia in ADTKD-HNF1B patients is frequently accompanied by hypocalciuria [72,73]. Several transcriptional targets of HNF1β have been identified, including the FXYD2 gene [72], which is involved in reabsorption of Mg²⁺ in the DCT, as described above. Therefore, inactivating mutations of HNF1β would lead to reduced expression of FXYD2 and, consequently, to renal Mg²⁺ wasting and hypomagnesemia [72]. HNF1β also regulates the transcription of KCNJ10, a gene that can affect Mg²⁺ transport in the DCT, as described above [77].

Transient neonatal hyperphenylalaninemia and primapterinuria

Transient neonatal hyperphenylalaninemia and primapterinuria (TNHP, OMIM #264070) is an autosomal recessive disorder characterized by mild transient hyperphenylalaninemia and elevated urinary levels of 7-biopterin [78]. Affected individuals are asymptomatic and exhibit normal psychomotor development. A follow-up study of TNHP patients showed that patients may also develop hypomagnesemia with renal Mg²⁺ wasting and MODY type diabetes [79]. TNHP is caused by mutations in the PCBD1 gene, which encodes the bifunctional protein pterin-4 α-carbinolamine dehydratase (PCBD1). PCBD1 functions as a cytosolic enzyme that is implicated in the regeneration of the essential cofactor tetrahydrobiopterin as well as a coactivator of HNF1β-mediated transcription within the nucleus [80]. Gene expression studies combined with immunohistochemical analysis showed that in the kidney, PCBD1 is expressed predominantly in the DCT [79]. PCBD1 interacts with the dimerization domain of HNF1β and regulates the formation of a transcriptionally active tetrameric complex [81]. Binding of PCBD1 to HNF1β stimulates the FXYD2 promoter in the DCT, and PCBD1 mutations identified in TNHP patients cause defective dimerization and degradation of the PCBD1 protein, leading to decreased FXYD2 promoter activity [79]. The reduced expression of FXYD2 would cause hypomagnesemia in these patients.

Kenny-Caffey syndrome type 2

Kenny-Caffey syndrome type 2 (KCS type 2, #OMIM 127000) is characterized by severe short stature, impaired skeletal development, eye abnormalities, hypomagnesemia, and hypoparathyroidism [82,83]. KCS type 2 patients may also have frequent episodes of low Ca²⁺ levels in serum triggered by hypoparathyroidism. This multisystem disease is caused by heterozygous missense mutations in the FAM111A gene, which encodes the nuclear trypsin-like serine protease FAM111A [82,83]. FAM111A is involved in the regulation of PTH production, calcium homeostasis, bone development and growth, but the specific mechanisms have not been determined [82,83]. FAM111A mutations identified in patients usually appear de novo, but some cases with autosomal dominant inheritance have been described [84]. These mutations affect the peptidase domain of FAM111A and may impair its catalytic activity [83,85].

FAM111A, first identified as an antiviral restriction factor, is ubiquitously expressed, and its nuclear localization suggests that it might be involved in transcriptional regulation [82,83,86]. FAM111A mutations result in hyperactivation of the FAM111A intrinsic protease activity, which could cause abnormal degradation of DNA-binding proteins or FAM111A depletion through hyper-autoproteolytic cleavage [87–89]. Hyperactive FAM111A is cytotoxic, disrupting nuclear structure and pore distribution in a protease-dependent manner [89]. Targets of FAM111A protease activity have been recently identified and include nucleoporins and the associated germinal center-associated nuclear protein transcription/replication factor [89]. Hypomagnesemia in KCS type 2 patients could be attributed to degradation of transcription factors involved in magnesium homeostasis. Tan et al. [90] suggested a potential role of FAM111A in regulation of CaSR, since KCS type 2 shares phenotypic characteristics with ADHH-like hypocalcemia and hypoparathyroidism.

Hypertension, hypercholesterolemia, and hypomagnesemia

This disorder was identified in a large pedigree and includes hypertension, hypercholesterolemia, and hypomagnesemia (OMIM #500005) [94]. Affected individuals also have hypocalciuria and hypokalemia. Each of these traits was transmitted via the maternal lineage with a pattern indicating mitochondrial inheritance. Other clinical characteristics include migraine headache, sensorineural hearing loss, and hypertrophic cardiomyopathy, all usually associated with mitochondrial dysfunction. Sequence analysis of the mitochondrial genome in the maternal lineage of the pedigree identified a C to T transition in the MT-TI gene, which encodes isoleucine transfer RNA (tRNA^Ile) [94]. Further analysis of affected members revealed that all copies of the mtDNA contain this mutation. The affected C is located immediately 5’ to the tRNA^Ile anticodon, and biochemical studies showed that the substitution of T significantly weakens ribosome binding [95]. These studies suggest that this mutation results in the loss of mitochondrial function. Hypomagnesemia associated with hypocalciuria points to a primary defect in the DCT [96].

Kearns-Sayre syndrome

Kearns-Sayre syndrome (KSS, OMIM #530000) is a rare progressive multisystem disease characterized by ophthalmoparesis/ptosis and pigmentary retinopathy. The onset is typically before 20 years of age, and patients typically present one of the following: cerebellar ataxia, cardiac conduction defects, deafness, short stature, cognitive involvement, tremor, and cardiomyopathy [97]. Some cases develop hypoparathyroidism and renal tubular dysfunction resulting in severe hypomagnesemia, hypocalcemia with hypermagnesuria, and hypokalemia [98,99]. KSS is caused by large deletions in mtDNA, which can reduce considerably ATP production [93]. In most cases, the deletions arise de novo but some are transmitted through maternal inheritance. Patients’ cells usually contain a mixture of wild-type and mutant mtDNA molecules in variable quantities, which is critical in determining the level of cellular dysfunction [92]. A defect in Mg²⁺ reabsorption in the TAL or DCT, due to ATP depletion, could be the cause of hypomagnesemia in these patients.

Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome

Hyperuricemia, pulmonary hypertension, renal failure and alkalosis (HUPRA) syndrome (OMIM #613845) is an autosomal recessive disease characterized by early-onset progressive renal failure, hyperuricemia, metabolic alkalosis, pulmonary hypertension, developmental delay, and, in some cases, hypomagnesemia [100]. This rare disorder has been diagnosed in only six children from three families and it is caused by homozygous missense mutation in SARS2 on chromosome 19, which encodes the mitochondrial seryl-tRNA synthetase (SARS2) [100,101]. SARS2 catalyzes the serine aminoacylation of two mitochondrial tRNAs. Only two mutations have been identified in patients with HUPRA syndrome, p.Asp390Gly and p.Arg402His. The p.Asp390Gly mutation significantly reduces the aminoacylation of one mitochondrial tRNA leading to its degradation, which would cause alterations in the synthesis of mitochondrial proteins and consequently in energy supply [100]. Decreased energy production may account for diminished Na⁺, K⁺-ATPase activity in the TAL and DCT, which could explain the salt wasting and hypomagnesemia observed in HUPRA patients.