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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...

MPSIDisease.com | MPS I Disease Spectrum

www.mps1disease.com/en/patients/about/disease-spectrum.aspx

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 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 ...

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

patient.info/doctor/hurlers-syndrome

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  ...

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 ...

OMIM Entry - # 607014 - HURLER SYNDROME

www.omim.org/entry/607014

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

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 ...

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 ...

Clinical manifestation of Hurler syndrome in a 7 year old child - NCBI

www.ncbi.nlm.nih.gov/pmc/articles/PMC3341767/

Mucopolysaccharidosis type I (MPS I H, Hurler syndrome) is a rare .... It is also important for couples with a family history of Hurler syndrome to undergo genetic  ...

mucopolysaccharidosis type I - Genetics Home Reference

ghr.nlm.nih.gov/condition/mucopolysaccharidosis-type-i

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

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Hurler syndrome: MedlinePlus Medical Encyclopedia

medlineplus.gov

Hurler syndrome is a type of mucopolysaccharidosis called MPS I. It is the most ... You have a family history of Hurler syndrome and are considering having ...

MPS I | MPS Society

mpssociety.org

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

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