Iread with interest the article “Brain and Spinal MR Imaging Findings in
Mucopolysaccharidoses: A Review” 1 and would like to illustrate optic canal narrowing in a …

Introduction: We report a case of retinal and posterior ocular findings in a 33-year-old man
diagnosed with Hunter syndrome (Mucopolysaccharidosis type II) in a multimodal imaging …

Hunter's syndrome (mucopolysaccharidosis(MPS) type II) is a rare X-linked recessive
metabolic disorder caused by deficiency in alpha-L-iduronatesulphate sulphatase.' …

We report imaging findings in a 3-year-old boy with the typical mild type of Hunter's disease.
MRI revealed multifocal large cyst-or spindle-like areas of increased and decreased signal …

Magnetic resonance imaging (MRI) of the brain (A) axial T2-weighted image,(B) coronal T2-
FLAIR weighted image, and (C) ultrasonography of the left eye of a 3-year-old boy who …

Magnetic resonance imaging (MRI) of the brain, neck and cervical spine of five patients with
the mild variant of Hunter's syndrome (iduronate sulphate sulphatase deficiency …

Hunter syndrome (mucopolysaccharidosis ii) is a rare X-linked lysosomal storage disease
caused by deficiency of the enzyme iduronate-2-sulfatase. The condition is one of a group of …

Discussion First described by Charles Hunter in 1917, HS is an X-linked recessive type II
mucopolysaccharidosis (MPS) characterized by deficient or absent enzyme iduronate-2 …

Purpose Purpose: Mucopolysaccharidosis (MPS) type II (Hunter syndrome) is a variable,
progressive, multisystem disorder including severe airway obstruction, cardiomyopathy …

Cervical Myelopathy Secondary to Hunter Syndrome in an Adult Page 1 of July 19, 2023. This
information is current as syndrome in an adult. Cervical myelopathy secondary to Hunter M …