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. The inability to break down these molecules results in a wide variety of symptoms caused by damage to several different organ systems, including but not limited to the nervous system, skeletal system, eyes, and heart.
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GargoylismHunter-Hurler diseaseHunter-Hurler syndromeHurler's SyndromeHurler's diseaseHurler's syndromeHurler SyndromeHurler diseaseHurler syndrome (MPS I)LipochondrodystrophyMucopolysaccharidosis, type IMucopolysaccharidosis IMucopolysaccharidosis I H (Hurler)Mucopolysaccharidosis IhMucopolysaccharidosis iPfaundler syndrome
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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. The inability to break down these molecules results in a wide variety of symptoms caused by damage to several different organ systems, including but not limited to the nervous system, skeletal system, eyes, and heart.
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Hurler syndrome, also known as ...... ndrome is autosomal recessive.
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differential diagnosis
DiseasesDB
eMedicine subject
ped
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eMedicine topic
1031
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geneReviewsId
geneReviewsName
Mucopolysaccharidosis Type I
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MedlinePlus
MeSH ID
OMIM id
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1,024,533,318
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Structure of dermatan sulfate, ...... es of Hurler syndrome patients
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causes
Deficiency of the alpha-L iduronidase enzyme
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differential
Hurler-Scheie syndrome; Scheie syndrome; Hunter syndrome; other mucopolysaccharidoses
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DiseasesDB
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ped
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GeneReviewsName
Mucopolysaccharidosis Type I
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GeneReviewsNBK
NBK1162
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ICD
MedlinePlus
MeshID
D008059
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name
Hurler syndrome
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OMIM
prognosis
3.786912E8
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Hurler syndrome, also known as ...... letal system, eyes, and heart.
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label
Hurler syndrome
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Hurler syndrome
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