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Síndrome de Morquio - Symptom

Nombres alternativos

Mucopolisacaridosis tipo IVA; Deficiencia de galactosamina-6-sulfatasa; Mucopolisacaridosis tipo IVB; Deficiencia de beta galactosidasa; MPS IV

Síntomas:

Pruebas y exámenes:

El médico llevará a cabo un examen físico y pruebas que pueden revelar:

Generalmente, primero se hacen los exámenes de orina que pueden mostrar mucopolisacáridos adicionales, pero que no pueden determinar la forma específica de MPS.

Otros exámenes pueden abarcar:

A las personas con el síndrome de Morquio se les debe hacer una resonancia magnética de la parte baja del cráneo y la parte superior del cuello para determinar si las vértebras superiores están subdesarrolladas.

  • Reviewed last on: 5/15/2011
  • Chad Haldeman-Englert, MD, Wake Forest School of Medicine, Department of Pediatrics, Section on Medical Genetics, Winston-Salem, NC. Review provided by VeriMed Healthcare Network. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.

Referencias

National Institute of Neurological Disorders and Stroke. Mucolipidoses Fact Sheet. Office of Communications and Public Liaison. Bethesda, MD; Publication No. 03-5115. February 13, 2007.

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