Impaired glucose tolerance in Fanconi-Bickel syndrome: Eight patients with two novel mutations
Fanconi-Bickel syndrome (FBS) is a rare, autosomal recessive disorder of carbohydrate metabolism caused by defects in the facilitative glucose transporter 2 (GLUT2 or SLC2A2) gene. Prominent findings are failure to thrive, renal tubular acidosis, hypoglycemia and postprandial hyperglycemia even mim...
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| Главные авторы: | , , , , , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Hacettepe University Institute of Child Health
2017-08-01
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| Серии: | The Turkish Journal of Pediatrics |
| Предметы: | |
| Online-ссылка: | https://turkjpediatr.org/article/view/1011 |
| Метки: |
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