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Pediatriya - Zhurnal im G.N. Speranskogo, ISSN 0031-403X, 2016, Volume 95, Issue 1, pp. 137 - 139
Journal Article
The Journal of Pediatrics, ISSN 0022-3476, 11/2019, Volume 214, pp. 151 - 157.e6
To clarify clinical and genetic features of Japanese children with congenital chloride diarrhea (CCD). This was a multi-institutional, retrospective survey of... 
polyhydramnios | Bartter syndrome | congenital intestinal atresia | salt substitution | SLC26A3 | dilated fetal bowel loops | DIAGNOSIS | DISEASE | FETUS | PEDIATRICS | BUTYRATE | MUTATIONS | ASSOCIATION | CHILDREN | Molecular genetics | Diarrhea | Genetic disorders
Journal Article
Alimentary Pharmacology & Therapeutics, ISSN 0269-2813, 02/2010, Volume 31, Issue 4, pp. 477 - 485
Journal Article
Pediatric health, medicine and therapeutics, ISSN 1179-9927, 2019, Volume 10, pp. 153 - 156
Congenital chloride diarrhea of infancy is a life threatening disease. We discuss two boys with congenital chloride diarrhea over a long time period before and... 
congenital chloride diarrhea | corticosteroid therapy
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 07/2018, Volume 63, Issue 8, pp. 887 - 892
Pseudo-Bartter/Gitelman syndrome (p-BS/GS) encompasses a clinically heterogeneous group of inherited or acquired disorders similar to Bartter syndrome (BS) or... 
DIFFERENTIAL-DIAGNOSIS | PANEL | CHANNEL | GENE | GENETICS & HEREDITY | COTRANSPORTER | SALT-LOSING TUBULOPATHIES | HYPOKALEMIC ALKALOSIS | MUTATIONS | Congenital diseases
Journal Article
Journal of Obstetrics and Gynaecology Research, ISSN 1341-8076, 11/2019, Volume 45, Issue 11, pp. 2280 - 2283
Journal Article
The Indian Journal of Pediatrics, ISSN 0019-5456, 8/2016, Volume 83, Issue 8, pp. 859 - 861
Journal Article
Rossijskij Vestnik Perinatologii i Pediatrii, ISSN 1027-4065, 04/2018, Volume 63, Issue 2, pp. 73 - 78
Chloride diarrhea is a rare genetically determined disease caused by mutations of the SLC26A3 gene and characterized by the appearance of persistent watery... 
treatment | hypokalemia | differential diagnosis | children | congenital chloride diarrhea | SLC26A3 gene | hypochloraemia | metabolic alkalosis
Journal Article
Journal Article