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Morquio Syndrome: A case report. Papirex

Publication Type : Journal Article

Publisher : Indian Journal of Research.

Source : Indian Journal of Research. Feb 2017 6(2):373-375

Url : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5935432/#:~:text=Case%20presentation,the%20maternal%20or%20paternal%20side.

Campus : Faridabad

Year : 2017

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.

Cite this Research Publication : Dudeja R, Gaba S, Gupta RK, Kumar A, Goel L, Das S. Morquio Syndrome: A case report. Papirex Indian Journal of Research. Feb 2017 6(2):373-375

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