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Issue: Vol.6 No.1 - January 2012
Gitelman’s syndrome presented with tetany: a case report
Authors: Md. Zahid Alam,

Affiliations: Department of Cardiology, Bangladesh Institute of Research & Rehabilitation in Diabetes Endocrine and Metabolic Disorders (BIRDEM), Shahbag, Dhaka, Bangladesh

AMB Safdar,

Affiliations: Department of Cardiology, Bangladesh Institute of Research & Rehabilitation in Diabetes Endocrine and Metabolic Disorders (BIRDEM), Shahbag, Dhaka, Bangladesh

Shabnam Jahan Hoque,

Affiliations: Department of Cardiology, Bangladesh Institute of Research & Rehabilitation in Diabetes Endocrine and Metabolic Disorders (BIRDEM), Shahbag, Dhaka, Bangladesh

Rownak Jahan Tamanna,

Affiliations: Department of Cardiology, Bangladesh Institute of Research & Rehabilitation in Diabetes Endocrine and Metabolic Disorders (BIRDEM), Shahbag, Dhaka, Bangladesh

Rowsan Ara,

Affiliations: Department of Cardiology, Bangladesh Institute of Research & Rehabilitation in Diabetes Endocrine and Metabolic Disorders (BIRDEM), Shahbag, Dhaka, Bangladesh

MM Zahurul Alam Khan

Affiliations: Department of Cardiology, Bangladesh Institute of Research & Rehabilitation in Diabetes Endocrine and Metabolic Disorders (BIRDEM), Shahbag, Dhaka, Bangladesh

Gitelman’s syndrome is an autosomal recessive disorder caused by a defect of the thiazide-sensitive sodium chloride co-transporter at the distal tubule, characterized by hypomagnesemia, hypokalemic alkalosis and hypocalciuria. We report a case of Gitlman’s syndrome in a 44 years old female patient who presented with generalized muscle weakness and carpal spasm and characteristic electrolyte abnormalities. This condition is sometimes confused with Bartter’s syndrome.

Ibrahim Med. Coll. J. 2012; 6(1): 34-36

Key words: Gitelman’s syndrome, tetany

Address for Correspondence:Dr. Md. Zahid Alam, Junior consultant, Department of Cardiology (Room: 813), BIRDEM Hospital, 122 Kazi Nazrul Islam Avenue, Shahbagh, Dhaka-1000, email: ilazybear@yahoo.com