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

Journal of Inherited Metabolic Disease
Christian J HendrikszElizabeth A Braunlin

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.

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Citations

Feb 14, 2013·Journal of Inherited Metabolic Disease·Guirish A SolankiChristian J Hendriksz
Feb 12, 2014·Orphanet Journal of Rare Diseases·Hsiang-Yu LinShuan-Pei Lin
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Methods Mentioned

BETA
light scattering
scanning electron microscopy
fiber optic bronchoscopy
enzyme replacement therapy
sedation

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