Literature DB >> 22565078

Novel biochemical abnormalities and genotype in Farber disease.

Mamta Muranjan1, Shruti Agarwal, Keya Lahiri, Murali Bashyam.   

Abstract

Farber disease caused by acid ceramidase deficiency is characterised by a triad of painful and swollen joints, subcutaneous nodules, and laryngeal involvement. A one year old female with overlapping features of the classical and type 5 variants is reported. Sialuria and elevated plasma chitotriosidase were unusual findings. A novel mutation of the ASAH 1 gene was detected from DNA extracted from the umbilical stump.

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Year:  2012        PMID: 22565078

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


  4 in total

1.  The face of lysosomal storage disorders in India: a need for early diagnosis.

Authors:  Shruti Agarwal; Keya Lahiri; Mamta Muranjan; Nirmal Solanki
Journal:  Indian J Pediatr       Date:  2014-12-09       Impact factor: 1.967

2.  Acid ceramidase treatment enhances the outcome of autologous chondrocyte implantation in a rat osteochondral defect model.

Authors:  M E Frohbergh; J M Guevara; R P Grelsamer; M F Barbe; X He; C M Simonaro; E H Schuchman
Journal:  Osteoarthritis Cartilage       Date:  2015-10-30       Impact factor: 6.576

Review 3.  Acid ceramidase deficiency: Farber disease and SMA-PME.

Authors:  Fabian P S Yu; Samuel Amintas; Thierry Levade; Jeffrey A Medin
Journal:  Orphanet J Rare Dis       Date:  2018-07-20       Impact factor: 4.123

Review 4.  Immunomodulatory Effects of Chitotriosidase Enzyme.

Authors:  Mohamed A Elmonem; Lambertus P van den Heuvel; Elena N Levtchenko
Journal:  Enzyme Res       Date:  2016-01-03
  4 in total

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