Please use this identifier to cite or link to this item: http://cris.unibe.edu.do/handle/123456789/309
Title: Morquio syndrome: a case report
Autores: Ramphul, K.
González Mejías, Stephanie
Ramphul, Y.
Researchers (UNIBE): González Mejías, Stephanie 
Affiliations: Facultad de Ciencias de la Salud 
Research area: Ciencias de la Salud
Keywords: Morquio syndrome; Mucopolysaccharidosis
Issue Date: 2018
Publisher: Cureus, Inc.
Source: Cureus, 10(3), e2270
Journal: Cureus 
Volume: 10
Issue: 3
Start page: e2270
Abstract: 
Mucopolysaccharidosis type IV (MPS IV), also known as Morquio syndrome, is a rare autosomal recessive lysosomal storage disease. The main features include skeletal defects and possible cardiopulmonary complications. The cost of diagnosing and treating this condition is high, and treatment is not easily available everywhere. We present a case of Morquio syndrome seen in a seven-year-old male from Iraq with multiple skeletal deformities.
URI: http://cris.unibe.edu.do/handle/123456789/309
DOI: 10.7759/cureus.2270
Appears in Collections:Publicaciones de la Facultad de Ciencias de la Salud

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