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  1. Hurler Syndrome - Cleveland Clinic

    • Hurler syndrome is the most severe form of MPS 1, a genetic condition that affects how cells break down sugar molecules. Learn about the symptoms, causes, diagnosis and treatment of this rare and life-th… 展开

    What Is Hurler Syndrome?

    Hurler syndrome is the most severe form of mucopolysaccharidosis type 1 (MPS 1). It’s an autosomal recessivecondition. MPS 1 is a condition where your body doesn't have enough enzyme… 展开

    Cleveland Clinic
    What Are Other Types of Mucopolysaccharidosis Type I?

    There are three types of Mucopolysaccharidosis type I (MPS I), including: 1. Hurler syndrome. 2. … 展开

    Cleveland Clinic
    Who Does Hurler Syndrome Affect?

    Hurler syndrome can affect any child since it's the result of a genetic mutationthat occurs randomly. If you have a history of mucopolysaccharidosis type I (MPS I) in your family, you’r… 展开

    Cleveland Clinic
     
  1. Mucopolysaccharidoses | National Institute of …

    2024年7月19日 · Mucopolysaccharidoses (MPS) are a group of disorders that affect the body's ability to break down and recycle complex molecules called glycosaminoglycans. MPS causes progressive cellular damage, organ …

  2. Mucopolysaccharidoses (MPS) - Johns Hopkins Medicine

    MPS is a group of genetic disorders that cause sugar to be excreted in urine and affect the brain, organs and joints. Learn about the symptoms, diagnosis and treatment of MPS and its orthopaedic complications.

  3. Mucopolysaccharidosis - Wikipedia

    Mucopolysaccharidosis (MPS) is a group of metabolic disorders caused by the absence or malfunctioning of enzymes that break down sugar molecules called glycosaminoglycans. MPS affects appearance, physical abilities, organ and …

  4. Mucopolysaccharidosis I (MPS I) - Hurler Syndrome and Scheie

  5. MPS Type I, Hurler Disease: Symptoms, Causes, Life …

    MPS I (mucopolysaccharidosis type 1) is a metabolic disorder caused by mutations in the gene that encodes alpha-L-iduronidase. It affects the breakdown of glycosaminoglycan, a major constituent of connective tissue, and causes …

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  7. Mucopolysaccharidosis type I - MedlinePlus

    MPS I is a condition that affects many parts of the body and causes enlarged organs, skeletal abnormalities, vision loss, and intellectual disability. It is caused by mutations in the gene that …

  8. Mucopolysaccharidosis Type 1 (MPS 1) - Children's Hospital of …

  9. What is MPS? | Muenzer MPS Center - UNC School of …

    MPS Defined Mucopolysaccharidoses (MPS) are a group of ultra-rare genetic disorders. Individuals with MPS are missing a specific enzyme involved in the breakdown/recycling of glycosaminoglycans, which are long chains of sugar …

  10. MPS conditions - MPS Society

    MPS conditions are rare, life limiting disorders that affect the breakdown of mucopolysaccharides in the body. Learn about the different types of MPS diseases, their symptoms, causes and …