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

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.

scholarly journals A Case Report on Neonatal Bartter Syndrome and It’s Effective Management-Clinical Pharmacist Perspective

2015 ◽  
Vol 8 (3) ◽  
pp. 133-135 ◽  
Author(s):  
Kandimalla Chaitanya ◽  
Chandra Jahnavi ◽  
Yerragundla Kanthi Kiran ◽  
Apollo James ◽  
T. Raman Ashok Kumar ◽  
...  
Keyword(s):  
Case Report ◽  
Clinical Pharmacist ◽  
Bartter Syndrome ◽  
Effective Management ◽  
Neonatal Bartter Syndrome

scholarly journals A UNUSAL PRESENTATION OF BARTTER SYNDROME

2019 ◽  
pp. 5-6
Author(s):  
Nitharsha Prakash M ◽  
N Nag Anand
Keyword(s):  
Case Report ◽  
Acute Gastroenteritis ◽  
Bartter Syndrome ◽  
Infants And Children ◽  
Renal Tubules ◽  
Adult Onset ◽  
Congenital Disease ◽  
Salt Wasting

Bartter Syndrome is a rare congenital disease that manifests as hypokalemia, hyponatremia and hypotension. The disease occurs due to defective genes that are responsible for the reabsorption of certain electrolytes in the renal tubules. Hence it results in salt-wasting dyselectrolytemia. By its inheritable nature, the usual presentation of the disease is in the infants and children. But this case report presents an adult with symptoms of Bartter Syndrome which was discovered by chance while the patient was being treated for Acute gastroenteritis. Adult onset of Bartter Syndrome is incredibly rare and has been reported only in few other cases.

scholarly journals Fetal urine biochemistry in antenatal Bartter syndrome: a case report

2016 ◽  
Vol 4 (9) ◽  
pp. 876-878 ◽  
Author(s):  
Myriam L. Rachid ◽  
Sophie Dreux ◽  
Isabelle Czerkiewicz ◽  
Georges Deschênes ◽  
Rosa Vargas‐Poussou ◽  
...  
Keyword(s):  
Case Report ◽  
Bartter Syndrome ◽  
Fetal Urine ◽  
Urine Biochemistry

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 Cystinosis Presenting with Findings of Bartter Syndrome - Case Report

2011 ◽  
Vol 3 (2) ◽  
pp. 101-104 ◽  
Author(s):  
Behzat Özkan ◽  
Atilla Çayır ◽  
Celalettin Koşan ◽  
Handan Alp
Keyword(s):  
Case Report ◽  
Bartter Syndrome

Classical Bartter syndrome – A case report

2015 ◽  
Vol 6 (3) ◽  
pp. 116-118
Author(s):  
Lalit Prakash Mali ◽  
Shyam Sundar Meena ◽  
Mukesh Baniwal
Keyword(s):  
Case Report ◽  
Bartter Syndrome
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