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genetic or congenital, metabolic
frequency
rare (U.S.)
likelihood by age
likelyhood by duration of symptoms
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The results are computer generated suggestions to help you find a physician. MEDgle does not recommend any particular type of physician or claim to be complete or accurate in the providers and specialties suggested.

Definition for Hurler Syndrome

Hurler syndrome, also known as mucopolysaccharidosis type I (MPS I) or "Hurler's disease", is a genetic disorder that results in the deficiency of alpha-L iduronidase, which is an enzyme that breaks down mucopolysaccharides. more


some common symptoms
delayed development
difficulty breathing
heart murmur
stomach swelling


some related diagnoses
1 - 7 of 176 diagnoses
congenital abnormalities coronary arteries
thalassemia intermedia
Pickwickian Syndrome
congenital heart disease
hereditary spherocytosis
Factor V Leiden thrombophilia
hyperkalemia
  more

do i have 'Hurler Syndrome'?
In addition the following diagnostic tests might be need to help verify the diagnosis:
diagnostic test search results for 'hurler syndrome'
1 - 5 of 28 diagnostic tests
Molecular Genetic Studies
ECHOcardiogram
EKG
Electrocardiogram
Hearing test
standard technique of representing hearing loss
X-rays
for more please login, login is free (click to login)



therapeutic procedures for 'Hurler Syndrome'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for Hurler Syndrome:


medications search results for 'hurler syndrome'
1 - 2 of 2 medications
rankings are computer generated. please consult your health care provider.
  bone marrow transplantation
  Laronidase



web search results for hurler syndrome
Results 1 - 50 - Hurler Syndrome
adam.about.com - summary
www.nlm.nih.gov - summary
adam.about.com - summary
www.ncbi.nlm.nih.gov - summary
www.ncbi.nlm.nih.gov - summary
en.wikipedia.org - summary







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