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A novel MAGED2 variant in a Chinese preterm newborn with transient antenatal Bartter’s syndrome with 4 years follow-up



Transient antenatal Bartter’s syndrome caused by MAGED2 mutation is a rare X-linked recessive renal tubular disorder. Cases reported are mostly infants, and the long-term prognosis of the disease is still under investigation.

Case presentation

We encountered a preterm male infant with polyhydramnios, polyuria, salt loss, hypercalciuria, nephrocalcinosis and alkalosis. Antenatal Bartter’s syndrome was suspected, but these clinical symptoms surprisingly disappeared after about 2 months. This led to the clinical diagnosis of transient antenatal Bartter’s syndrome. Gene analysis in this patient disclosed a novel variant (c.1598C > T, p.Ala533Val) in exon 12 of MAGED2 gene, and his mother was a heterozygous carrier. This patient was followed up in clinic for 4 years without recurrence of imbalance of potassium, sodium and chloride. His height and weight were in normal range, and all laboratory examinations and nephrotic ultrasound were also normal.


We reported the first Chinese case of transient antenatal Bartter’s syndrome caused by MAGED2 mutation. The 4-year follow-up of our case further demonstrates the benign prognosis of the disease and indicates that early recognition of this phenotype could avoid unnecessary treatments.

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Antenatal Bartter’s syndrome is an inherited disorder, characterized by polyuria, failure to thrive, hypokalemia, metabolic alkalosis, hyperreninemia and renal salt wasting which need lifelong fluid and electrolyte supplementation as well as nonsteroidal anti-inflammatory drugs. Some severe cases show mental retardation. The defective chloride transport in the loop of Henle leads to fetal polyuria resulting in severe hydramnios and premature delivery.

However, some case reports described male infants’ antenatal Bartter’s syndrome spontaneously resolved within several weeks after birth [1]. Laghmani et al. identified a genetic cause of this transient antenatal phenotype, MAGED2 mutations by whole-exome sequencing of the suspected X chromosome [2]. The transient antenatal Bartter’s syndrome patients present with polyhydramnios, prematurity and renal salt tubular function, but these clinical manifestations disappeared completely in a few months after birth. Most patients reported were infants, and the long-term influence on kidney function was still unknown [3].

We identified a novel variant (c.1598C > T, p.Ala533Val) in MAGED2 by next generation sequencing in a Chinese preterm neonate with transient antenatal Bartter’s syndrome phenotype. This patient was followed up in clinic for 4 years with regular test of kidney function and ultrasound.

Case presentation

A previously healthy 31-year-old G1P0 woman presented with polyhydramnios at 22 weeks (amniotic fluid volume 11.5 cm, normal value < 8 cm) which led to a preterm delivery of a male infant at 29 weeks. The boy weighed 1480 g (P85) and was 38.5 cm (P50) long with head circumference 26.5 cm (P61). Polyuria (mean 5.8 ml/kg.h) was observed immediately after birth. Dehydration and rapid weight loss (decrease 25% at the fourth day after birth) followed. Persistent hyponatremia, hypokalemia, hypochloremia (Na+ 129 mmol/L, K+ 2.95 mmol/L, Cl 94 mmol/L) necessitated intravenous fluid infusion and supplemental electrolytes. Elevated levels of renin and angiotonin (PRA1 > 12 ng/ml/h, normal value range 0.05–0.79 ng/ml/h, AT-II1 > 800 pg/ml, normal value range 16.2-64 pg/ml) were noted. Severe hypercalciuria was identified by the ratio of Urine calcium:creatinine, which was 1147.8 mg/g Cr, and it further caused medullary nephrocalcinosis. Metabolic alkalosis progressively developed (maximal pH 7.521, BE 7.8 mmol/L, HCO3 31.1 mmol/L). The magnesium level in blood remained normal. Fortunately, he passed hearing screening by Otoacoustic emissions (OAE) and Auditory brainstem response (ABR). There was no positive family history for those symptoms.

Antenatal Bartter’s syndrome was suspected. He was treated with parenteral nutrition containing Na+ (maximum 4 mmol/kg, adjusting according to the concentration of Na+) and K+ (maximum 4.4 mmol/kg, adjusting according to the concentration of K+) until 21 days after birth. And then, oral 15% KCl solution (2 ml, three times per day, reduced gradually 3 weeks later), and spironolactone (2 mg/d) were given for about 1 month. All symptoms gradually relieved. Neonatal polyuria normalized within 4 days, and metabolic alkalosis disappeared after 1 month. After 2 months, serum electrolyte maintained normal without oral supplemental. Renin and angiotonin level also decreased to normal (PRA1 0.79 ng/ml/h, AT-II1 82.33 pg/ml) and kidney ultrasound showed improvement of medullary nephrocalcinosis. He weighed 3890 g (P40) and was 53 cm (P51) long with head circumference 35.5 cm (P53) at corrective gestational age of 42 weeks. Then, this patient was evaluated in clinic every 12 months. In the most recent follow-up when he was 4 years old, his height was 106.4 cm and weight was 15.8 kg. Complete blood test and kidney function tests were normal (Hgb 122 g/L, Na 138 mmol/L, K 4.0 mmol/L, Cl 103 mmol/L, creatine 31 μmol/L). kidney ultrasound revealed normal kidney size and structure.

A congenital nephropathy gene panel including genes of classic and antenatal Bartter’s syndrome (270 genes listed in supplemental Table 1) was used to detect the pathogenic mutation. Genomic DNA was extracted from peripheral blood leukocytes of this patient and his parents according to the standard protocols for sequencing. On analysis of MAGED2 gene, a variation(c.1598C > T, p.Ala533Val) detected by Next generation sequencing was confirmed by Sanger sequencing analyses (Fig. 1). This patient is hemizygous and his mother was a heterozygous carrier.

Fig. 1
figure 1

Sanger sequencing of MAGED2 gene in proband and family member. Blood samples were collected from the patient as well as his parents, and sequenced. Mutated MAGED2 gene (c.1598C > T) was found in the patient 1 while his mother was a heterozygous carrier for that mutation

Discussion and conclusions

In antenatal Bartter’s syndrome, five different genes are found to be responsible: SLC12A19 (type I), KCNJ1 (type II), BSND (type IV), CLCNKA, and CLCNKB (type IVb) [4]. Clinical manifestations include polyhydramnios, prematurity, polyuria, and renal salt wasting. Sensorineural deafness is also a manifestation of antenatal Bartter’s syndrome type IV and IVb. Treatment of lifelong electrolyte supplementation and nonsteroidal anti-inflammatory drugs is needed.

In May 2016, MAGED2 was defined to be responsible for transient antenatal Bartter’s syndrome. MAGED2 is located in Xp11.2 which is a hot spot for X-linked mental retardation (XLMR) and encodes melanoma-associated antigenD2 (MAGE-D2). MAGE-D2 is expressed universally in normal tissues and participates in cell cycle regulation. It protects cells from apoptosis [5]. This gene has been proven participating in development of breast cancer and melanoma and may be a promising biomarker for gastric cancer [6,7,8]. Laghmani et al. found MAGE-D2 also expresses in the distal tubules in kidneys and promotes NKCC2 and NCC expression through adenylate cyclase and cAMP signaling and a heat-shock protein [2]. Recent study reveals that MAGED2 mRNA and protein are significantly upregulated in tubular cells in human kidney injury, which indicates MAGED2 plays a role in tubular cell injury during acute kidney disease [9].

Most patients reported were infants, and the longest follow-up was 17 years with normal glomerular and tubular function [2]. All symptoms disappeared spontaneously during follow-up, but the mechanism of transient character of the disease is not clear. Two hypotheses were made by Laghmani et al. [2]. First, beyond a certain stage of renal development, MAGED2 is not needed for the expression of NKCC2 and NCC because of the increased sensitivity of adenylate cyclase activity to vasopressin. In addition, postnatally higher levels of oxygenation in the kidney may promote the synthesis of NKCC2 and NCC [10].

Various kinds of mutations associated with transient antenatal Bartter’s syndrome including nonsense, frameshift, splice-site mutations, missense and in-frame deletion, were identified and reported [2, 3, 11]. In this patient, a missense mutation was present. The variation, c.1598C > T locates in exon 12 of the MAGED 2 gene. It predicts a change from an alanine codon to a valine codon. This variant was not found in the 1000 Genomes ( and Exac (, suggesting that it was not likely to be a Single Nucleotide Polymorphism (SNP). Polyphen-2 software was used to further evaluate the possible deleterious consequence of the novel MAGED2missense variant, and the p.Ala533Val substitution was predicted to be possibly damaging with a score of 0.780 which suggest the novel variant would substantially alter the function of protein. The results of multiple amino acid sequence alignment showed that the novel p.Ala533Val variant occurred at a highly evolutionarily conserved residue. Further study is needed to reveal the subsequent protein structure and functional change.

In this patient, diagnosis was made based on the transient clinical manifestations of antenatal Bartter’s syndrome. The differential diagnosis of this Bartter-like phenotype is other known types of antenatal Bartter’s syndrome (types I, II, IV, and IVb). According to the clinical manifestations of 13 patients with transient antenatal Bartter’s syndrome described by Laghmani et al., polyhydramnios appeared in second trimester of pregnancy, which was earlier than other known types of antenatal Bartter’s syndrome. All 13 patients with transient antenatal Bartter’s syndrome were preterm caused by polyhydramnios [2]. Polyuria lasted about 3 days to 6 weeks and ended at 30 to 33 weeks of gestational age. This phenotype is probably life threatening because of dehydration according to the reported cases. Bartter’s syndrome types I, II, IV, and IVb are associated with similar manifestations like polyhydramnios, prematurity. But polyuria, hypokalemia, and metabolic alkalosis persist and need lifelong treatment [12]. However, after 4-year follow-up in our hospital, our patient did not show any relapse of this diseases, suggesting a favorable prognosis of transient antenatal Bartter’s syndrome if the patient received carefully supporting treatment during the acute phase of this disease. Thus, we highlight the importance of early recognition of transient antenatal Bartter’s syndrome for saving lives as well as avoiding unnecessary and potentially harmful indomethacin treatment.

In conclusion, we report here the first Chinese case of transient antenatal Bartter’s syndrome and a novel MAGED2 gene alteration. Gene analysis is recommended for preterm infant with prenatal severe polyhydramnios, postnatal polyuria and hypokalemia. Our 4 years follow-up of the patient further demonstrates a favorable prognosis of the disease and thus, early recognition of this transient disease helps to avoid unnecessary treatments.

Availability of data and materials

A congenital nephropathy gene panel including genes of classic and antenatal Bartter’s syndrome (270 genes listed in supplemental Table 1) for next generation sequencing was used to detect the pathogenic mutation. The primers and conditions for thermal cycling, and the datasets used during the study are available from the corresponding author on reasonable request.



Auditory brainstem response


Otoacoustic emissions


melanoma-associated antigen D2


X-linked mental retardation


  1. 1.

    Reinalter S, Devlieger H, Proesmans W. Neonatal Bartter syndrome: spontaneous resolution of all signs and symptoms. Pediatr Nephrol. 1998;12(3):186–8.

    CAS  Article  PubMed  Google Scholar 

  2. 2.

    Laghmani K, Beck BB, Yang SS, Seaayfan E, Wenzel A, Reusch B, et al. Polyhydramnios, transient antenatal Bartter's syndrome, and MAGED2 mutations. N Engl J Med. 2016;374(19):1853–63.

    CAS  Article  PubMed  Google Scholar 

  3. 3.

    Legrand A, Treard C, Roncelin I, Dreux S, Bertholet-Thomas A, Broux F, et al. Prevalence of novel MAGED2 mutations in antenatal Bartter syndrome. Clin J Am Soc Nephrol. 2018;13(2):242–50.

    Article  PubMed  Google Scholar 

  4. 4.

    Alfandary H, Landau D. Future considerations based on the information from Barrter's and Gitelman's syndromes. Curr Opin Nephrol Hypertens. 2017;26(1):9–13.

    CAS  Article  PubMed  Google Scholar 

  5. 5.

    Barker PA, Salehi A. The MAGE proteins: emerging roles in cell cycle progression, apoptosis, and neurogenetic disease. J Neurosci Res. 2002;67(6):705–12.

    CAS  Article  PubMed  Google Scholar 

  6. 6.

    Pirlot C, Thiry M, Trussart C, Di Valentin E, Piette J, Habraken Y. Melanoma antigen-D2: a nucleolar protein undergoing delocalization during cell cycle and after cellular stress. Biochim Biophys Acta. 2016;1863(4):581–95.

    CAS  Article  PubMed  Google Scholar 

  7. 7.

    Tseng HY, Chen LH, Ye Y, Tay KH, Jiang CC, Guo ST, et al. The melanoma-associated antigen MAGE-D2 suppresses TRAIL receptor 2 and protects against TRAIL-induced apoptosis in human melanoma cells. Carcinogenesis. 2012;33(10):1871–81.

    CAS  Article  PubMed  Google Scholar 

  8. 8.

    Kanda M, Nomoto S, Oya H, Takami H, Shimizu D, Hibino S, et al. The expression of melanoma-associated antigen D2 both in surgically resected and serum samples serves as clinically relevant biomarker of gastric Cancer progression. Ann Surg Oncol. 2016;23(Suppl 2):S214–21.

    Article  PubMed  Google Scholar 

  9. 9.

    Valino-Rivas L, Cuarental L, Agustin M, Husi H, Cannata-Ortiz P, Sanz AB, et al. MAGE genes in the kidney: identification of MAGED2 as upregulated during kidney injury and in stressed tubular cells. Nephrol Dial Transplant. 2019;34(9):1498–507.

    CAS  Article  PubMed  Google Scholar 

  10. 10.

    Quigley R, Saland JM. Transient antenatal Bartter's syndrome and X-linked polyhydramnios: insights from the genetics of a rare condition. Kidney Int. 2016;90(4):721–3.

    Article  PubMed  Google Scholar 

  11. 11.

    Yang K, Huo X, Zhang Y, Zhang M, Gao Y, Wu D, et al. Genetic analysis of a pedigree affected with Bartter's syndrome. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019;36(7):701–3.

    Article  PubMed  Google Scholar 

  12. 12.

    Koulouridis E, Koulouridis I. Molecular pathophysiology of Bartter's and Gitelman's syndromes. World J Pediatr. 2015;11(2):113–25.

    CAS  Article  PubMed  Google Scholar 

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Many thanks to the patient and his parents.


National Key Research and Development Project of China (2016YFC0901500 and 2016YFC0905102), which supports genetic test.

Author information




MS M and MQ Z drafted the manuscript. Y Z and ZH L clinically evaluated and managed the patients medically. F Y and M W carried out the molecular genetic testing as well as analysis. ZQ Q critically revised the final manuscript for important intellectual content and approved it. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Zhenghong Li or Zhengqing Qiu.

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Ethical no: ZJS-1248. Approved by the Institutional Review Board of Peking Union Medical College Hospital (PUMCH). Written informed consent was obtained from the mother.

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Written informed consent was obtained from parents for the publication of all personal information contained in this case report.

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Ma, M., Zhang, M., Zhou, Y. et al. A novel MAGED2 variant in a Chinese preterm newborn with transient antenatal Bartter’s syndrome with 4 years follow-up. BMC Nephrol 22, 408 (2021).

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  • MAGED2 gene
  • Transient antenatal Bartter’s syndrome
  • Polyhydramnios
  • Case report