Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Fanconi-Bickel syndrome
Introduction
Synonyms and keywords: Fanconi-Bickel syndrome
Overview
Overview
Glycogen storage disease type XI is a form of glycogen storage disease.
It is also known as “Fanconi-Bickel syndrome”, for Guido Fanconi and Horst Bickel.[1][2]
References
References
- ↑ Template:WhoNamedIt
- ↑ FANCONI G, BICKEL H (1949). “Not Available”. Helv Paediatr Acta (in Undetermined). 4 (5): 359–96. PMID 15397919. Unknown parameter
|month=ignored (help) - ↑ Santer R, Schneppenheim R, Suter D, Schaub J, Steinmann B (1998). “Fanconi-Bickel syndrome–the original patient and his natural history, historical steps leading to the primary defect, and a review of the literature”. Eur. J. Pediatr. 157 (10): 783–97. PMID 9809815. Unknown parameter
|month=ignored (help) - ↑ Santer R, Steinmann B, Schaub J (2002). “Fanconi-Bickel syndrome–a congenital defect of facilitative glucose transport”. Curr. Mol. Med. 2 (2): 213–27. PMID 11949937. Unknown parameter
|month=ignored (help) - ↑ Santer R, Groth S, Kinner M; et al. (2002). “The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome”. Hum. Genet. 110 (1): 21–9. doi:10.1007/s00439-001-0638-6. PMID 11810292. Unknown parameter
|month=ignored (help)
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]