A Case of Fanconi-Bickel Syndrome with Mild Clinical Signs / 대한내과학회지
Korean Journal of Medicine
;
: 210-213, 2013.
Article
Dans Coréen
| WPRIM
| ID: wpr-63514
ABSTRACT
Fanconi-Bickel syndrome is a rare autosomal recessive disorder caused by a mutation in the facilitative glucose transporter 2 gene (GLUT2 or SLC2A2 gene) that codes for the glucose transporter protein 2 expressed in hepatocytes, pancreatic beta-cells, enterocytes, and renal tubular cells. Mutation of this gene leads to defective carbohydrate metabolism, hepatomegaly, glucose intolerance, proximal renal tubular dysfunction, and hypophosphatemic rickets. We report a case of Fanconi-Bickel syndrome in an 18-year-old man who presented due to renal glycosuria; a mutation was identified in the GLUT2 gene (c.482C > A + c.1556G > A). To the best of our knowledge, unlike previous reports of Fanconi-Bickel syndrome, this case was relatively unusual in that it caused only mild clinical signs.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Intolérance au glucose
/
Entérocytes
/
Hépatocytes
/
Transporteurs de glucose par diffusion facilitée
/
Transporteur de glucose de type 2
/
Métabolisme glucidique
/
Rachitisme hypophosphatémique familial
/
Syndrome de Fanconi
/
Hépatomégalie
Type d'étude:
Etude diagnostique
langue:
Coréen
Texte intégral:
Korean Journal of Medicine
Année:
2013
Type:
Article
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