Literature DB >> 8233358

Cataracts in Morquio syndrome (mucopolysaccharidosis IV A).

H Olsen1, K Baggesen, A K Sjolie.   

Abstract

Three siblings with Morquio syndrome (mucopolysaccharidosis IV A) are described. In addition to the characteristic dwarfism with skeletal deformities, odontoid anomalies, hearing loss and corneal clouding, the authors found almost identical lens opacities in all three patients. Lenticular opacities have not previously been described in patients with Morquio's syndrome IV A.

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Year:  1993        PMID: 8233358     DOI: 10.3109/13816819309042908

Source DB:  PubMed          Journal:  Ophthalmic Paediatr Genet        ISSN: 0167-6784


  4 in total

1.  Morquio syndrome: electron microscopic findings.

Authors:  T Leslie; M A R Siddiqui; D A Aitken; C M Kirkness; W R Lee; A I Fern
Journal:  Br J Ophthalmol       Date:  2005-07       Impact factor: 4.638

Review 2.  Clinical overview and treatment options for non-skeletal manifestations of mucopolysaccharidosis type IVA.

Authors:  Christian J Hendriksz; Maisoon Al-Jawad; Kenneth I Berger; Sara M Hawley; Rebecca Lawrence; Ciarán Mc Ardle; C Gail Summers; Elizabeth Wright; Elizabeth Braunlin
Journal:  J Inherit Metab Dis       Date:  2012-02-23       Impact factor: 4.982

Review 3.  International guidelines for the management and treatment of Morquio A syndrome.

Authors:  Christian J Hendriksz; Kenneth I Berger; Roberto Giugliani; Paul Harmatz; Christoph Kampmann; William G Mackenzie; Julian Raiman; Martha Solano Villarreal; Ravi Savarirayan
Journal:  Am J Med Genet A       Date:  2014-10-24       Impact factor: 2.802

4.  Ophthalmologic manifestations in Taiwanese patients with mucopolysaccharidoses.

Authors:  Hsiang-Yu Lin; Wei-Chun Chan; Lee-Jen Chen; Yuan-Chieh Lee; Shu-I Yeh; Dau-Ming Niu; Pao Chin Chiu; Wen-Hui Tsai; Wuh-Liang Hwu; Chih-Kuang Chuang; Shuan-Pei Lin
Journal:  Mol Genet Genomic Med       Date:  2019-03-08       Impact factor: 2.183

  4 in total

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