Abstract:Fanconi-Bickel Syndrome (FBS) is an autosomal recessive disorder caused by mutations in SLC2A2 gene, encoding a facilitative glucose transporting membrane protein. Its phenotype can vary, and is characterized by short stature, hepatomegaly, fasting hypoglycemia, impaired glucose tolerance, hyperlipidemia, and tubular nephropathy. So far, over 100 cases in the world have been reported, and only three cases of childbearing. The authors describe a case of a 39-year-old woman affected by FBS with a spontaneous pre… Show more
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