Morquio syndrome. Case report
Abstract
We present a case of a Morquio syndrome, it is a disease transmitted by inheritance autosomic recessive, is systemic disease, mainly affects cartilage, clinically there is deficiency of Galactose-6-sulfatase and beta-galactosidase enzymes, clinically is observed disharmonic growth of bones and coarse fascies.Downloads
References
Instituto (le errores inuatos del metabolismo lEEM. Facultad de Ciencias, Pontificia Universidad Javeiiana. Disponible en: http;//www.javeriana.edu.co/ieim/ caitillas/ morquio.htm
Rodríguez E, Gómez A. Mucopolisacaiidosis. Salud UIS 2003; 35: 135-144.
Biología virtual. Disponible en: http://www.viitual.unal.edu.co/cursos/Ciencias/2000024/lecciones/cap01/01_01_05.htm Univirtual. Universidad Nacional de Colombia. 2009.
Bravermau N, Hoover-Foug J. Mucopolysaccharidosis Type IV. Disponible en: http://www.emedicine.coni/ped/topic 1477.htm,2003
Echeverri O, Barrera LA, Bermúdez MC. Mucopolisacaiidosis IH (síndrome de Hurler). Primeros casos en Colombia. Colomb Med 1995; 26(3): 89-92.
Moua S.A, Alice K. Abdel-Aleem, Ahmed IS. EL-Katouiyl, et al. Clinical, antropometric, radiological and molecular characteristics of Egyptian achondroplasia patients. Egypt J. Med Hum. Genet. 2009; 10(1). Disponible en: http://ajol.info/rndex.php/ejhg/issue/view/6267
Mena M, Obaudo R. Síndrome de Morquio. Revista Chilena de Pediatría 1976;47(3):247-253