Neonatal Bartter syndrome - use of indomethacin in the newborn period and prevention of growth failure

1996 ◽  
Vol 10 (6) ◽  
pp. 756-758 ◽  
Author(s):  
E. M. Hodson ◽  
L. P. Roy ◽  
J. F. Knight ◽  
F. E. Mackie
Keyword(s):  
Growth Failure ◽  
Bartter Syndrome ◽  
Newborn Period ◽  
Neonatal Bartter Syndrome

Neonatal Bartter syndrome with unilateral multicystic dysplastic kidney disease

2003 ◽  
Vol 18 (4) ◽  
pp. 391-393
Author(s):  
Takuji Tomimatsu ◽  
Hirotsugu Fukuda ◽  
Toru Kanzaki ◽  
Shinya Hirano ◽  
Kazuko Wada ◽  
...  
Keyword(s):  
Kidney Disease ◽  
Bartter Syndrome ◽  
Multicystic Dysplastic Kidney ◽  
Dysplastic Kidney ◽  
Neonatal Bartter Syndrome ◽  
Multicystic Dysplastic Kidney Disease

scholarly journals Neonatal Bartter syndrome: A case report from Northern India

2021 ◽  
pp. 10-14
Author(s):  
Astitva Singh ◽  
Nishant Sharma ◽  
Prachi Agarwal ◽  
Bolledu Swaroop Anand ◽  
Akshay Shukla
Keyword(s):  
Case Report ◽  
Genetic Disorder ◽  
Failure To Thrive ◽  
Bartter Syndrome ◽  
Thick Ascending Limb ◽  
Older Children ◽  
Northern India ◽  
Tubular System ◽  
Renal Tubular ◽  
Neonatal Bartter Syndrome

Abstract. Bartter Syndrome is a rare genetic disorder affecting the renal tubular system causing a decreased absorption of sodium and chloride in the thick ascending limb of the Henle loop. Most children present in infancy with complaints of polyuria, polydipsia, vomiting, constipation and failure to thrive while older children present with recurrent episodes of dehydration, muscle weakness and cramps. The present study aimed to demonstrate a case of Bartter syndrome presenting as acute gastroenteritis.

PP-89. Neonatal Bartter syndrome: Case report

2010 ◽  
Vol 86 ◽  
pp. S53
Author(s):  
Neslihan Cicek Deniz ◽  
Turgut Agzıkuru ◽  
Yasemin Akın ◽  
Fatma Kaya Narter ◽  
Melek Kose
Keyword(s):  
Case Report ◽  
Bartter Syndrome ◽  
Neonatal Bartter Syndrome

Humoral factor in children with neonatal Bartter syndrome reduces bone calcium uptake in vitro

1998 ◽  
Vol 12 (5) ◽  
pp. 371-376 ◽  
Author(s):  
Lawrence R. Shoemaker ◽  
William Bergstrom ◽  
Kevin Ragosta ◽  
Thomas R. Welch
Keyword(s):  
Calcium Uptake ◽  
Bartter Syndrome ◽  
Humoral Factor ◽  
Bone Calcium ◽  
Neonatal Bartter Syndrome

Two novel mutations of the gene for Kir 1.1 (ROMK) in neonatal Bartter syndrome

1998 ◽  
Vol 12 (1) ◽  
pp. 69-71 ◽  
Author(s):  
Martin Vollmer ◽  
Martin Koehrer ◽  
Rezan Topaloglu ◽  
Brigitte Strahm ◽  
Heymut Omran ◽  
...  
Keyword(s):  
Bartter Syndrome ◽  
Novel Mutations ◽  
Neonatal Bartter Syndrome

scholarly journals Status epilepticus as the only presentation of the neonatal Bartter syndrome

2012 ◽  
Vol 16 (2) ◽  
pp. 300 ◽  
Author(s):  
Soumya Patra ◽  
MithunC Konar ◽  
Rajarshi Basu ◽  
AjoyK Khaowas ◽  
Soumyadeep Dutta ◽  
...  
Keyword(s):  
Status Epilepticus ◽  
Bartter Syndrome ◽  
Neonatal Bartter Syndrome

scholarly journals Neonatal Bartter Syndrome

2016 ◽  
Vol 36 (2) ◽  
pp. 204-207 ◽  
Author(s):  
Amrita Roy ◽  
Debalina Sarkar Chakraborty ◽  
Shivani Dogra ◽  
Sudip Sengupta
Keyword(s):  
Caesarean Section ◽  
Metabolic Alkalosis ◽  
Bartter Syndrome ◽  
High Serum ◽  
Emergency Caesarean Section ◽  
Male Baby ◽  
Emergency Caesarean ◽  
Neonatal Bartter Syndrome

The neonatal form of Bartter syndrome is characterized by intrauterine onset of polyuria leading to severe polyhydramnios. We report a case of a 31 weeks, male baby was born by emergency Caesarean Section due to severe polyhydramnios (AFI 54). Postnatally, baby had polyuria, dehydration, hyponatremia, hypokalemia and hypochloremic metabolic alkalosis. Possibility of neonatal Bartter syndrome was supported by high serum renin and aldosterone levels. Correction of electrolytes and dehydration along with indomethacin constituted the treatment. This syndrome is reported to make paediatricians aware about the severe neonatal form of the disease.J Nepal Paediatr Soc 2016;36(2):204-207.

Growth hormone deficiency in children with antenatal Bartter syndrome

2019 ◽  
Vol 32 (3) ◽  
pp. 225-231 ◽  
Author(s):  
Inna Spector-Cohen ◽  
Ariel Koren ◽  
Waheeb Sakran ◽  
Yardena Tenenbaum-Rakover ◽  
Rephael Halevy
Keyword(s):  
Growth Retardation ◽  
Growth Failure ◽  
Failure To Thrive ◽  
Poor Response ◽  
Bartter Syndrome ◽  
Hormone Deficiency ◽  
Gh Therapy ◽  
Poor Growth ◽  
Presenting Symptoms ◽  
Stimulation Tests

Abstract Background Bartter syndrome is a group of rare autosomal-recessive renal disorders characterized by hypokalemic hypochloremic metabolic alkalosis associated with severe growth failure; the exact causes for growth retardation are unclear. GH deficiency (GHD) has been reported in a few cases of Bartter syndrome. The aim of our study was to determine the prevalence of GHD in children with antenatal Bartter syndrome and to assess their response to GH therapy. Methods Ten patients aged 1.5–14.5 years and diagnosed with antenatal Bartter syndrome were enrolled. Seven children with short stature underwent GH stimulation tests. Results Common presenting symptoms were failure to thrive and polyuria. The mean patient height at study entry was −2.7 standard deviation (SD) (range 0.89 to −5.95) and mean weight (SD) was −1.7 (range 1.89 to −4.11). A decline in height and weight (SD) was observed over the years. GHD was diagnosed in four children and GH therapy was started in all of them. Two patients responded very well and gained >1 SD in height, one patient stopped therapy due to non-adherence and one had a poor response. Conclusions In addition to other important causes for poor growth in antenatal Bartter syndrome, our findings suggest that GHD should also be considered as a cause of growth retardation and therefore, clinical assessment of the GH axis is recommended. GH therapy has a role in the treatment of growth failure in some individuals with Bartter syndrome.

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