A rare case of severe Hunter's Syndrome

Hunter's Syndrome or mucopolysaccharidosis Type II is a rare metabolic disorder caused by the deficiency of lysosomal enzyme iduronate-2-sulfatase. It results in progressive accumulation of deramatan and heparan sulfates in tissues leading to a wide clinical spectrum of systemic manifestations....

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Egile Nagusiak: Sharon Vincent (Egilea), Joe Mathew Cherian (Egilea), Abi M Thomas (Egilea), Rajesh Kumar (Egilea)
Formatua: Liburua
Argitaratua: Wolters Kluwer Medknow Publications, 2018-01-01T00:00:00Z.
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