Literature DB >> 17413201

Fanconi-Bickel syndrome.

Sunil Karande1, Nilesh Kumbhare, Madhuri Kulkarni.   

Abstract

We present here the first case of Fanconi-Bickel syndrome, a rare type of glycogen storage disease, from India. A 17-month-old female child presented with severe growth retardation and abdominal distention. Clinical examination revealed a "doll-like" face, massive hepatomegaly, and rickets. Laboratory investigations confirmed severe hypophosphatemic rickets and proximal renal tubular dysfunction. Liver biopsy showed glycogen accumulation in the hepatocytes.

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Year:  2007        PMID: 17413201

Source DB:  PubMed          Journal:  Indian Pediatr        ISSN: 0019-6061            Impact factor:   1.411


  5 in total

1.  Fanconi-Bickel syndrome in a 3-year-old Indian boy with a novel mutation in the GLUT2 gene.

Authors:  Arun Gopalakrishnan; Manish Kumar; Sriram Krishnamurthy; Osamu Sakamoto; Sadagopan Srinivasan
Journal:  Clin Exp Nephrol       Date:  2011-05-31       Impact factor: 2.801

2.  Hypophosphatemic rickets: presenting features of fanconi-bickel syndrome.

Authors:  Mahua Roy; K Bose; D K Paul; Puja Anand
Journal:  Case Rep Pathol       Date:  2011-10-18

3.  Fanconi-Bickel syndrome - mutation in SLC2A2 gene.

Authors:  Mohit Kehar; Sunita Bijarnia; Sian Ellard; Jayne Houghton; Renu Saxena; I C Verma; Nishant Wadhwa
Journal:  Indian J Pediatr       Date:  2014-06-10       Impact factor: 1.967

Review 4.  Fanconi-Bickel Syndrome: A Review of the Mechanisms That Lead to Dysglycaemia.

Authors:  Sanaa Sharari; Mohamad Abou-Alloul; Khalid Hussain; Faiyaz Ahmad Khan
Journal:  Int J Mol Sci       Date:  2020-08-31       Impact factor: 5.923

5.  Fanconi-Bickel syndrome in a Ugandan child - diagnostic challenges in resource-limited settings: a case report.

Authors:  Thereza Piloya; Hawa Ssematala; Lydia Paparu Dramani; Oliva Nalikka; Miriam Baluka; Victor Musiime
Journal:  J Med Case Rep       Date:  2020-09-30
  5 in total

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