Novel solute carrier family 26, member 3 mutation in a prenatal recurrent case with congenital chloride diarrhea

Author:

Wu Siqi12,Han Jin123ORCID,Zhang Yongling3,Ye Zhichao1,Lu Ping1,Tian Kege1

Affiliation:

1. Department of Prenatal DiagnosisDongguan Kanghua Hospital Dongguan China

2. Department of Obstetrics and GynecologyGuangzhou Medical University Guangzhou China

3. Department of Prenatal diagnosisGuangzhou Women and Children's Medical Center Guangzhou China

Funder

The Science and Technology Program of Dongguan

The Science and Technology Program of Guangdong

The Science and Technology Program of Guangzhou

Publisher

Wiley

Subject

Obstetrics and Gynecology

Reference15 articles.

1. Congenital chloride diarrhea, an autosomal recessive disease

2. Familial chloride diarrhoea (congenital alkalosis with diarrhoea);Davidson AG;Aust Paediatr J,1972

3. Congenital Chloride Diarrhea (CCD): A Case Report of CCD Suspected by Prenatal Ultrasonography and Magnetic Resonance Imaging (MRI)

4. Colonic electrolyte transport in health and in congenital chloride diarrhea.

5. Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea;Moseley RH;Am J Physiol,1999

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