Searching for Hurler Syndrome Support information? Find all needed info by using official links provided below.
https://rarediseases.info.nih.gov/diseases/12559/hurler-syndrome
97 rows · Mar 01, 2014 · Management is multidisciplinary. Hematopoietic stem cell transplantation (HSCT) is the treatment of choice for patients with Hurler syndrome under 2.5 years of age (and in selected patients over this age limit) as it can prolong survival, preserve neurocognition, and ameliorate some somatic features. HSCT should be performed early in the disease course, before developmental …
https://mpssociety.org/learn/diseases/mps-i/
MPS I (Hurler-Scheie syndrome ) is caused by a recessive gene. There is a one in four chance with every pregnancy that the child will inherit the defective gene from each carrier parent and will be affected with the disease. There is a two in three chance that unaffected brothers and sisters of children with MPS I …
https://healthjade.net/hurler-syndrome/
What is Hurler syndrome. Hurler syndrome is the most severe form of mucopolysaccharidosis type 1 (MPS type 1), a rare lysosomal storage disease, characterized by skeletal abnormalities, cognitive impairment, heart disease, respiratory problems, enlarged liver and spleen, characteristic facies and reduced life expectancy.
https://www.webmd.com/children/mucopolysaccharidosis-i-mps-i
Mucopolysaccharidosis I (MPS I) is a rare genetic disorder that affects both physical and mental development and can cause organ damage.Author: Stephanie Watson
http://www.uptodate.com/contents/search?search=HURLER+SYNDROME
…Intrathecal ERT in a canine model of Hurler syndrome normalized GAG storage in the brain and decreased spinal meningeal storage . One patient with MPS I (Hurler syndrome) and progressive cognitive decline …
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