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Hurler syndrome

en.wikipedia.org/wiki/Hurler_syndrome

Hurler syndrome, also known as mucopolysaccharidosis type I (MPS I), Hurler's disease, also ... Genetic counseling can help parents who have a family history of the mucopolysaccharidoses determi...

Hurler syndrome: MedlinePlus Medical Encyclopedia

medlineplus.gov/ency/article/001204.htm

Experts recommend genetic counseling and testing for couples with a family history of Hurler syndrome who are considering having children. Prenatal testing is ...

Hurler Syndrome - Symptoms, Diagnosis, Treatment of Hurler ...

www.nytimes.com/health/guides/disease/hurler-syndrome/overview.html

May 7, 2013 ... Hurler syndrome is a rare, inherited disease of metabolism in which a ... with a family history of Hurler syndrome who are considering having ...

MPS I | MPS Society

mpssociety.org/mps/mps-i/

MPS I has also been called Hurler, Hurler-Scheie and Scheie syndrome . Hurler takes its name from Gertrude Hurler, the doctor who described a boy and girl ...

Hurler syndrome | Counsyl

www.counsyl.com/diseases/hurler-syndrome/

Hurler syndrome, also called mucopolysaccharidosis type I, is an inherited disease in which the body lacks an enzyme called alpha-L-iduronidase. Without this ...

Symptoms of Hurler syndrome - Be The Match

bethematch.org/for-patients-and-families/learning-about-your-disease/hurler-syndrome/symptoms-of-hurler-syndrome/

In Hurler syndrome, the body is missing an enzyme that breaks down large molecules called glycosaminoglycans (GAG). As GAG molecules build up in the body ...

OMIM Entry - # 607014 - HURLER SYNDROME

www.omim.org/607014

607014 - HURLER SYNDROME - MUCOPOLYSACCHARIDOSIS TYPE IH; ... Inheritance. Molecular Genetics. Population Genetics. Animal Model. History.

Hurler syndrome - Be The Match

bethematch.org/for-patients-and-families/learning-about-your-disease/hurler-syndrome/

In Hurler syndrome, the body has a defective gene and cannot make an important enzyme. Enzymes are proteins inside cells that break down larger building ...

Hurler Syndrome (MPS I) | The Oncofertility Consortium

oncofertility.northwestern.edu/resources/hurler-syndrome-mps-i

Feb 6, 2016 ... Hurler syndrome, a Mucopolysaccharidosis type 1 (MPS I) condition, occurs .... The natural history of MPS I: global perspectives from the MPS I ...

Hurler syndrome - Natural Living Center

www.naturallivingcenter.net/ns/DisplayMonograph.asp?StoreID=b571dewxvcs92jj200akhmccqa7w8v75&DocID=condition-hurlersyndrome

Hurler syndrome is a rare, inherited disorder in which a hereditary factor, or gene, .... Amniocentesis: When there is a family history of any of the three MPH I ...

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MPSIDisease.com | MPS I Disease Spectrum

www.mps1disease.com

The historical term for the most severe version of the disease is “Hurler disease” or "Hurler syndrome,” named after the doctor who first described this condition.

Hurler's Syndrome. What is hurler's syndrome? Information | Patient

patient.info

Home · Professional Reference; Hurler's Syndrome. Hurler's Syndrome .... Beck M, Arn P, Giugliani R, et al; The natural history of MPS I: global perspectives from  ...

mucopolysaccharidosis type I - Genetics Home Reference

ghr.nlm.nih.gov

Sep 20, 2016 ... This disorder was once divided into three separate syndromes: Hurler syndrome (MPS I-H), Hurler-Scheie syndrome (MPS I-H/S), and Scheie ...