Anna  Miskova,Dace  Rezeberga,Gita  Jansone,Kristīne  Rasnača,Laura Lūse,Natālija  Vedmedovska,Sabīne  Kovale,
Clinical Case of Pregnancy and Follow-Up of Bartter Syndrome (Type II) with a Novel Mutation
Case Reports in Obstetrics Gynecology and Reproductive
2020
2674-5070
http://dx.doi.org/10.31487/j.CROGR.2020.01.05
https://www.sciencerepository.org/clinical-case-of-pregnancy-and-follow-up-of-bartter-syndrome_CROGR-2020-1-105 
Abstract: Background: Bartter syndrome is a rare autosomal recessive inherited salt wasting tubulopathy, it`s
incidence proportion is 1.2 cases per 1.000.000 live births. The present case - report discusses a clinical case
of an antenatal Bartter syndrome (type II) with a novel mutation and it`s course from antenatal presentation
to 6 months postpartum.
Case Presentation: The case-report discusses a clinical case of an antenatal Bartter syndrome (type II) with
a novel homozygous missense variant mutation in KCNJ1 gene: c.554C>T (p. Pro185Leu). Symptoms
presented from 24 weeks of pregnancy as premature labour threats, maternal dyspnoea and severe
polyhydramnios (amniotic fluid index 36 cm). Therapeutic interventions included use of indomethacin,
dexamethasone, micronized progesterone and three consequent amnioreductions. Pregnancy was prolonged
until 32 weeks and induced due to severe reoccurring polyhydramnios, progressing maternal dyspnoea and
inability to perform next amnioreduction. Labour was complicated by severe placental abruption and new
born – boy was referred to neonatal intensive care unit. Neonatal period was complicated by electrolyte
abnormalities: hyponatremia, hypochloremic metabolic alkalosis, transient hyperkalaemia that gradually
developed into hypokalaemia, hypercalcemia and elevated rennin and aldosterone levels characteristic to
type II Bartter syndrome. At 6 months (corrected age 4 months) he is gaining weight within normal ranges
and his psychomotor development is ahead of his corrected age, without any need for daily medications.
Conclusion: The present case report describes the clinical course of a Bartter syndrome is of high
importance, due to the reason that it shows clinical course of patient with novel mutation and offers one of
the ways how to manage the disease. The described novel mutation may have favourable prognosis for
neonate. The pregnancy should be managed as high-risk pregnancy with expertise in perinatal diagnostics
and interventions. Early recognition, and interventions, are and essential to prolong a pregnancy and lessen
prematurity complications.Keywords: Neonatal Bartter syndrome, Type II Bartter syndrome, novel mutation, amnioreduction, case report, chorio-amniotic separation