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  2. Hunter syndrome - Wikipedia

    en.wikipedia.org/wiki/Hunter_syndrome

    Hunter syndrome is caused by a deficiency of the lysosomal enzyme iduronate-2-sulfatase (I2S). [2] [3] The lack of this enzyme causes heparan sulfate and dermatan sulfate to accumulate in all body tissues. [4] Hunter syndrome is the only MPS syndrome to exhibit X-linked recessive inheritance. [4] The symptoms of Hunter syndrome are comparable ...

  3. Lysosomal storage disease - Wikipedia

    en.wikipedia.org/wiki/Lysosomal_storage_disease

    (E76.0) Mucopolysaccharidoses, including Hunter syndrome and Hurler disease (E77) Glycoprotein storage disorders (E77.0-E77.1, E75.11) Mucolipidoses; Mucolipidosis IV is a gangliosidosis; Also, glycogen storage disease type II (Pompe disease) is a defect in lysosomal metabolism as well, [6] although it is otherwise classified into E74.0 in ICD-10.

  4. Mucopolysaccharidosis - Wikipedia

    en.wikipedia.org/wiki/Mucopolysaccharidosis

    Children may experience noisy breathing and recurring upper respiratory tract and ear infections. Feeding may be difficult for some children, and many experience periodic bowel problems. Children with Hurler syndrome often die before age 10 from obstructive airway disease, respiratory infections, and cardiac complications.

  5. Mucopolysaccharidosis type I - Wikipedia

    en.wikipedia.org/wiki/Mucopolysaccharidosis_type_I

    Most children develop limited language capabilities. Death usually occurs by age 10. [2] [3] In less severe cases, (Scheie syndrome, or attenuated MPS I), the presentation can vary considerably. Although symptoms generally begin to appear after age 5, the diagnosis is usually made after age 10.

  6. Hurler syndrome - Wikipedia

    en.wikipedia.org/wiki/Hurler_syndrome

    Hurler syndrome, also known as mucopolysaccharidosis Type IH (MPS-IH), Hurler's disease, and formerly gargoylism, is a genetic disorder that results in the buildup of large sugar molecules called glycosaminoglycans (GAGs) in lysosomes.

  7. Regenxbio's Hunter Syndrome Gene Therapy Shows Efficacy ... - AOL

    www.aol.com/news/regenxbios-hunter-syndrome-gene...

    Regenxbio Inc (NASDAQ: RGNX) has announced a safety update and additional positive interim data from its ongoing Phase 1/2 trial of RGX-121 to treat patients up to 5 years old diagnosed with ...

  8. Maroteaux–Lamy syndrome - Wikipedia

    en.wikipedia.org/wiki/Maroteaux–Lamy_syndrome

    Growth begins normally, but children usually stop growing by age 8. By age 10, children often develop a shortened trunk, crouched stance, and restricted joint movement. In more severe cases, children also develop a protruding abdomen and forward-curving spine. Skeletal changes, particularly in the pelvis, are progressive and limit movement.

  9. Elon Musk's X settles Donald Trump's free speech lawsuit ...

    www.aol.com/elon-musks-x-settles-donald...

    Donald Trump sued Twitter after being kicked off the platform following the Jan. 6 riots. Ally Elon Musk bought it, now X is reportedly settling.

  1. Related searches hunter syndrome in children icd 10

    hunter syndrome in children icd 10 code