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When their child was diagnosed with a genetic illness, Mark and Jeanne Dant raised more than $1 million for research. One of the scientists they funded developed an enzyme replacement that has ...
Every Tuesday, Niamh Condon has to miss a day of school. The 14-year-old, from Knocklong, Co Limerick, has a rare condition called Hurler-Scheie Syndrome, and she has to spend her day in Limerick ...
About MPS I (Hurler, Hurler-Scheie, Scheie syndrome) MPS I is an autosomal recessive lysosomal storage disorders (“LSD”) caused by a deficiency of α-L-iduronidase, ...
The federal health minister is vowing to help an 11-year-old boy with a rare genetic disorder whose family can't afford his treatments. Mackenzie Olsen has Hurler-Scheie syndrome, a genetic ...
Dr. Morton Cowan and Dr. Mohammad Diab of UCSF Medical Center discuss the ongoing procedures Kian must undergo, such as back surgery every six months so that his organs have room to grow, as well as ...
Children with Hurler syndrome experience progressive growth failure after hematopoietic cell transplantation (HCT). The goal of this study was to review the safety and efficacy of growth hormone ...
Stem cells hold hope for Hurler’s syndrome Date: November 6, 2013 Source: University of Adelaide Summary: Research using special adult stem cells is promising new hope for better treatments for ...
A deficiency of β-galactosidase (pH 5.0) was found in frozen tissues (brain, liver, kidney and spleen) from 10 patients with Hurler's syndrome (Types 1–3). The diminished activity of this ...
Between December 1995 and October 2002, 20 consecutive children with Hurler's syndrome received busulfan, cyclophosphamide, and antithymocyte globulin before receiving cord-blood transplants from ...
LONDON--(BUSINESS WIRE)--Technavio has announced its pipeline analysis report on the Hurler syndrome market. The report includes a detailed analysis of the pipeline molecules under investigation ...
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