| Literature DB >> 25523092 |
Farzaneh Abbasi1, Faezeh Azizi2, Mona Javaheri2, Asieh Mosallanejad3, Azadeh Ebrahim-Habibi4, Soudeh Ghafouri-Fard5.
Abstract
Fanconi-Bickel syndrome (FBS) is a rare autosomal recessive disorder characterized by hepatorenal glycogen accumulation, proximal renal tubular dysfunction, impaired utilization of glucose and galactose, rickets, and severe short stature. It has been shown to be caused by mutations in GLUT2 gene, a member of the facilitative glucose transporter family. Here, we report an Iranian family with 2 affected siblings. The clinical findings in the patients include developmental delay, failure to thrive, hepatomegaly, enlarged kidneys and rickets. A novel 6 nucleotide deletion (c.1061_1066del6, p.V355_S356del2) is shown to be segregated with the disease in this family.Entities:
Keywords: Fanconi–Bickel syndrome; GLUT2; Novel mutation
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Year: 2014 PMID: 25523092 DOI: 10.1016/j.gene.2014.12.024
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688