[The Fanconi-Bickel syndrome: one more case]
- PMID: 1635533
[The Fanconi-Bickel syndrome: one more case]
Abstract
The association of de Toni-Debré-Fanconi syndrome with alteration of galactose metabolism and glycogen hepatic storage, before further clarification, is defined as Fanconi-Bickel syndrome. The Authors present a case in which the alterations in galactose metabolism typically do not affect the enzymes responsible for galactosemia. In such patients a recognised enzymatic defect glycogenosis is not involved and glycogen storage in the liver can be a secondary phenomenon, which can increase, differing according to each subject. Liver biopsy to detect storage can be avoided when all the other diagnostic criteria are observed.
Similar articles
-
[The Fanconi-Bickel syndrome].Bol Med Hosp Infant Mex. 1991 Apr;48(4):255-60. Bol Med Hosp Infant Mex. 1991. PMID: 1867746 Spanish.
-
[Coexistence of liver glycogenosis, Fanconi's syndrome and abnormal galactose metabolism in a 3-year-old child].Pol Tyg Lek. 1980 Dec 29;35(52):2065-6. Pol Tyg Lek. 1980. PMID: 6945566 Polish. No abstract available.
-
Defective galactose oxidation in a patient with glycogen storage disease and Fanconi syndrome.Pediatr Res. 1983 Feb;17(2):157-61. doi: 10.1203/00006450-198302000-00015. Pediatr Res. 1983. PMID: 6572355
-
The glycogenoses and other inherited disorders of carbohydrate metabolism.Clin Perinatol. 1976 Mar;3(1):79-98. Clin Perinatol. 1976. PMID: 182428 Review. No abstract available.
-
[Fanconi-Bickel syndrome].Ryoikibetsu Shokogun Shirizu. 2001;(33):668-9. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462623 Review. Japanese. No abstract available.
Cited by
-
Diabetes-like renal glomerular disease in Fanconi-Bickel syndrome.Pediatr Nephrol. 1995 Jun;9(3):287-91. doi: 10.1007/BF02254185. Pediatr Nephrol. 1995. PMID: 7632512