Literature DB >> 19149988

Farber disease: a rare neurodegenerative disorder.

Ameer Ahmad1, Atta Ullah Mazhar, Muhammad Anwar.   

Abstract

This is the case report of a two-and-a-half-year old male infant with Farber disease, which is a rare neurodegenerative mucolipidosis. The child presented with regression of milestones, laryngeal involvement and painful joints with swellings around the joints. Neuroimaging findings and the biopsy of the soft tissue swellings helped to reach the diagnosis.

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Year:  2009        PMID: 19149988     DOI: 01.2009/JCPSP.6768

Source DB:  PubMed          Journal:  J Coll Physicians Surg Pak        ISSN: 1022-386X            Impact factor:   0.711


  4 in total

1.  Chronic lung injury and impaired pulmonary function in a mouse model of acid ceramidase deficiency.

Authors:  Fabian P S Yu; Diana Islam; Jakub Sikora; Shaalee Dworski; Jiří Gurka; Lucía López-Vásquez; Mingyao Liu; Wolfgang M Kuebler; Thierry Levade; Haibo Zhang; Jeffrey A Medin
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2017-11-22       Impact factor: 5.464

Review 2.  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

3.  Etiology and treatment of adrenoleukodystrophy: new insights from Drosophila.

Authors:  Hannah B Gordon; Lourdes Valdez; Anthea Letsou
Journal:  Dis Model Mech       Date:  2018-06-15       Impact factor: 5.758

4.  Deletion of MCP-1 Impedes Pathogenesis of Acid Ceramidase Deficiency.

Authors:  Fabian P S Yu; Shaalee Dworski; Jeffrey A Medin
Journal:  Sci Rep       Date:  2018-01-29       Impact factor: 4.379

  4 in total

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