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

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          Abstract

          Mucopolysaccharidosis type IVA (MPS IVA) or Morquio syndrome is a multisystem disorder caused by galactosamine-6-sulfatase deficiency. Skeletal manifestations, including short stature, skeletal dysplasia, cervical instability, and joint destruction, are known to be associated with this condition. Due to the severity of these skeletal manifestations, the non-skeletal manifestations are frequently overlooked despite their significant contribution to disease progression and impact on quality of life. This review provides detailed information regarding the non-skeletal manifestations and suggests long-term assessment guidelines. The visual, auditory, digestive, cardiovascular, and respiratory systems are addressed and overall quality of life as measured by endurance and other functional abilities is discussed. Impairments such as corneal clouding, astigmatism, glaucoma, hearing loss, hernias, hepatomegaly, dental abnormalities, cardiac valve thickening and regurgitation, obstructive sleep apnea, tracheomalacia, restrictive and obstructive respiratory compromise, and muscular weakness are discussed. Increased awareness of these non-skeletal features is needed to improve patient care.

          Electronic supplementary material

          The online version of this article (doi:10.1007/s10545-012-9459-0) contains supplementary material, which is available to authorized users.

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          Author and article information

          Contributors
          chris.hendriksz@bch.nhs.uk
          Journal
          J Inherit Metab Dis
          J. Inherit. Metab. Dis
          Journal of Inherited Metabolic Disease
          Springer Netherlands (Dordrecht )
          0141-8955
          1573-2665
          23 February 2012
          23 February 2012
          March 2013
          : 36
          : 2
          : 309-322
          Affiliations
          [ ]Birmingham Children’s Hospital NHS Foundation Trust, Birmingham, UK
          [ ]Institute of Dentistry, Queen Mary University London, London, UK
          [ ]André Cournand Pulmonary Physiology Laboratory, Bellevue Hospital, School of Medicine, New York University, New York, NY USA
          [ ]BioMarin Pharmaceutical Inc., Novato, CA USA
          [ ]Department of Ophthalmology, University of Minnesota, Minneapolis, MN USA
          [ ]Department of Pediatrics, University of Minnesota, Minneapolis, MN USA
          [ ]Clinical Inherited Metabolic Disorders, Birmingham Children’s Hospital NHS Foundation Trust, Steelhouse lane, Birmingham, B4 6NH UK
          Author notes

          Communicated by: Ed Wraith

          Article
          9459
          10.1007/s10545-012-9459-0
          3590399
          22358740
          8596b48e-9cb9-426b-9cb3-84b996a33411
          © The Author(s) 2012
          History
          : 23 November 2011
          : 18 January 2012
          : 24 January 2012
          Categories
          Review
          Custom metadata
          © SSIEM and Springer Science+Business Media Dordrecht 2013

          Internal medicine
          Internal medicine

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