Hurler-Scheie Syndrome (MPS I)

A Guide to Understanding Hurler, Hurler-Scheie and Scheie Syndrome (Mucopolysaccharidosis type I)
Source/Author: The National MPS Society 
Support Group
A booklet in pdf format on MPSI, discussing the cause, inheritance, prenatal diagnosis, clinical problems (divided by body system), general treatment and management and specific treatment of MPSI. Click on MPSI to download booklet.

Guia para entender los syndromes de Hurler, Hurler-Scheie and Scheie.
Source/Author: The MPS society 
Support Group
IN SPANISH 
A booklet in pdf format on MPSI, discussing the cause, inheritance, prenatal diagnosis, clinical problems (divided by body system), general treatment and management and specific treatment of MPSI. Click on MPSI to download booklet

Hurler syndrome
Source/Author: National Organization of Rare Diseases 
Web-based (medical)
Very brief description of the clinical features/characteristics, medical complications and genetics of this condition.

Intrathecal enzyme replacement therapy in a patient with mucopolysaccharidosis type I and symptomatic spinal cord compression.
Source/Author: Munoa-Rojas MV, Vieira T, Costa R, Fagondes S, John A, Barrach Jardim L, Vedolin LM, Raymundo M, Dickson PI, Kakkis E, Giugliani R
Abstract
Medical journal article on trial of enzyme replacement therapy injected directly into the spinal canal rather than the veins in a patient with Hunter syndrome. 
Full text article available by contacting [email protected]

Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis I.
Source/Author: Clarke LA, Wraith E, Beck M, Kolodny EH, Pastores CM, Muenzer J, Rapoport DM, Berger KI, Sidman M, Kakkis, ED, Cox GF
Abstract
Medical journal article on a study to evaluate the benefits and risks for Laronidase enzyme replacement therapy in patients with MPSI. 
Full text article available by contacting [email protected]

Mucopolisacaridosis, tipo 1
Source/Author: Michael Beck; Orphanet 
Web-based (medical)
IN SPANISH. 
Detailed overview of this condition in medical terminology.

Mucopolysaccharidose de type 1
Source/Author: Jean-Marie Saudubray; Orphanet 
Web-based (medical)
IN FRENCH. 
Detailed overview of this condition in medical terminology.

Mucopolysaccharidoses and anaesthetic risks.
Source/Author: Sjogren P, Pedersen T, Steinmetz H. Acta Anaesthesiol Scand. 1987 Apr;31(3):214-8. 
Abstract
Discussion of the risks that can be encountered when administering anesthesia to an individual with one of the MPS conditions

mucopolysaccharidosis (MPS) I
Source/Author: Jablonski Syndromes Database 
Web-based (medical)
Brief summary, features by body system, multiple references

Mucopolysaccharidosis type 1
Source/Author: Michael Beck; Orphanet 
Web-based (medical)
Detailed overview of this condition in medical terminology.

Mucopolysaccharidosis I: management and treatment guidelines.
Source/Author: Muenzer J, Wraith JE, Clarke LA and the International Consensus Panel on the Management and Treatment of Mucopolysaccharidosis I.
Abstract
Medical journal article on care management of MPS I. 
Full text article available by contacting [email protected]

Mucopolysaccharidosis Type I
Source/Author: Lorne A Clarke, MD and Jonathan Heppner, PhD candidate; Gene Reviews 
Web-based (medical)
Detailed discussion of the condition in medical terminology. Includes diagnosis, clinical description, differential diagnosis, management, genetic counseling, molecular genetics, resources.

Mucopolysaccharidosis Type I H/S
Source/Author: Maryam Banikazemi, MD; Medscape
Web-based (medical)
Description of condition in medical terminology, including clinical information, diagnosis, treatment and patient information.

Mucopolysaccharidosis, Type I
Source/Author: OMIM, Online Mendelian Inheritance in Man 
Web-based (medical)
Medical/Scientific description of MPS I (Hurler syndrome)with emphasis on the genetics of the condition

Mucopolysaccharidoses.
Source/Author: Muenzer J. Adv Pediatr. 1986;33:269-302. 
Abstract 
Overview of the MPS conditions.