Fanconi Bickel syndrome: clinical phenotypes and genetics in a cohort of Sudanese children

Fanconi-Bickel syndrome (FBS) is a rare condition of carbohydrate metabolism, caused by a recessive defect in the facilitative glucose transporter GLUT2 encoded by the SLC2A2 gene and characterized by a wide spec...

Source: International Journal of Pediatric Endocrinology - November 23, 2020 Category: Endocrinology Authors: Salwa A. Musa, Areej A. Ibrahim, Samar S. Hassan, Matthew B Johnson, Asmahan T. Basheer, Ali M. Arabi and Mohamed A. Abdullah Tags: Research Source Type: research