Neonatal Bartter syndrome: A case report from Northern India
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...
Main Authors: | Astitva Singh, Nishant Sharma, Prachi Agarwal, Bolledu Swaroop Anand, Akshay Shukla |
---|---|
Format: | Article |
Language: | English |
Published: |
State Institution «Institute of Nephrology NAMS of Ukraine"
2021-08-01
|
Series: | Український Журнал Нефрології та Діалізу |
Subjects: | |
Online Access: | https://ukrjnd.com.ua/index.php/journal/article/view/560 |
Similar Items
-
A case of Bartter syndrome type I with atypical presentations
by: Eun Hye Lee, et al.
Published: (2010-08-01) -
Nephrocalcinosis and Placental Findings in Neonatal Bartter Syndrome
by: Hidehiko Maruyama, et al.
Published: (2013-05-01) -
Anaesthesia for laparoscopic cholecystectomy in Bartter′s syndrome
by: Bala S Bhaskar, et al.
Published: (2010-01-01) -
A Case of Childhood-Onset Bartter Syndrome Type 1 with Renal Dysfunction
by: PENG Xiaoyan, et al.
Published: (2024-01-01) -
Bartter Type 4a Syndrome Diagnosed in a 30-week-old Preterm Neonate
by: Çağrı Cumhur Gök, et al.
Published: (2023-03-01)