Neonatal Bartter Syndrome Type 1
Hajer Aloulou*, Salma Ben Ameur*, Imen Zouch, Amira Bouraoui*, Sonia AbdelHak**, Rosa Vargas Poussou***, Thouraya Kammoun*, Mongia Hachicha*
*Department of Pediatrics, Sfax, Tunisia**, Laboratory of genetics-Pasteur Institut, Tunis ,Tunisia, *** Department of Genetics, European Hospital ,George, Pompidou.
Abstract

Bartter's syndrome is heterogeneous renal tubular disorder affecting sodium, potassium, chloride reabsorption in the thick ascending limb of Henle's loop. It is characterized by urinary potassium loss and metabolic alkalosis. BS type 1 also referred to as antenatal or neonatal BS, is caused by mutations in the SLC12A1 gene encoding bumetanide-sensitive-sodium-potassium-chloride cotransporter (NKCC2). In antenatal BS, abnormality begins in utero with fetal polyuria resulting in polyhydramnios and premature delivery. Another hallmark of this variant is a marked hypercalciuria and as a secondary consequence, the development of nephrocalcinosis and osteopenia. A 45 day old-boy born following a pregnancy complicated by severe polyhydramnios at a gestational age of 29 weeks, presented with fractures of upper limbs, dehydration, persistent hypokalemia, hypochloremic metabolic alkalosis with normal blood pressure, elevated plasma renin activity and nephrocalcinosis. Genetic study showed homozygosity mutations in the SLC12A1 gene.
Disclaimer: The information given by www.pediatriconcall.com is provided by medical and paramedical & Health providers voluntarily for display & is meant only for informational purpose. The site does not guarantee the accuracy or authenticity of the information. Use of any information is solely at the user's own risk. The appearance of advertisement or product information in the various section in the website does not constitute an endorsement or approval by Pediatric Oncall of the quality or value of the said product or of claims made by its manufacturer.
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.