Keyword Analysis & Research: mld


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mld1.720.98754933

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Keyword CPC PCC Volume Score
mld0.130.6606072

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  • Metachromatic leukodystrophy - Symptoms and causes - Mayo Clinic

    mayoclinic.org

    https://www.mayoclinic.org/diseases-conditions/metachromatic-leukodystrophy/symptoms-causes/syc-20354733

    WEBMar 6, 2020 · Metachromatic leukodystrophy is a rare hereditary (genetic) disorder that causes fatty substances (lipids) to build up in cells, particularly in the brain, spinal cord and peripheral nerves. This buildup is caused by a deficiency of an enzyme that helps break down lipids called sulfatides. The brain and nervous system progressively lose ...

    DA: 62 PA: 85 MOZ Rank: 70

  • Metachromatic Leukodystrophy: What It Is, Causes & Symptoms

    clevelandclinic.org

    https://my.clevelandclinic.org/health/diseases/6067-metachromatic-leukodystrophy

    WEBFeb 6, 2023 · Metachromatic leukodystrophy (MLD) is a genetic condition that causes a progressive decline in your mental and motor (movement) functions. Symptoms get worse over time. Treatment for the condition is mainly supportive and includes therapies like medication, occupational therapy and a feeding tube.

    DA: 11 PA: 80 MOZ Rank: 44

  • Metachromatic Leukodystrophy | National Institute of Neurological

    nih.gov

    https://www.ninds.nih.gov/health-information/disorders/metachromatic-leukodystrophy

    WEBNov 28, 2023 · Metachromatic leukodystrophy (MLD), also known as globoid cell leukodystrophy, is one of a group of genetic disorders characterized by the toxic buildup of lipids (fatty materials like oils and waxes) and other storage materials in cells in the white matter of the central nervous system and peripheral nerves.

    DA: 43 PA: 36 MOZ Rank: 80

  • Metachromatic leukodystrophy - Wikipedia

    wikipedia.org

    https://en.wikipedia.org/wiki/Metachromatic_leukodystrophy

    WEBMetachromatic leukodystrophy (MLD) is a lysosomal storage disease which is commonly listed in the family of leukodystrophies as well as among the sphingolipidoses as it affects the metabolism of sphingolipids.

    DA: 3 PA: 98 MOZ Rank: 21

  • Metachromatic leukodystrophy Information | Mount Sinai - New York

    mountsinai.org

    https://www.mountsinai.org/health-library/diseases-conditions/metachromatic-leukodystrophy

    WEBMetachromatic leukodystrophy (MLD) is a genetic disorder that affects nerves, muscles, other organs, and behavior. It slowly gets worse over time. Causes. MLD is usually caused by the lack of an important enzyme called arylsulfatase A (ARSA).

    DA: 18 PA: 71 MOZ Rank: 73


  • Metachromatic Leukodystrophy (MLD) | UPMC Children's Hospital

    chp.edu

    https://www.chp.edu/our-services/rare-disease-therapy/conditions-we-treat/metachromatic-leukodystrophy

    WEBMetachromatic leukodystrophy (MLD) is a disease passed from parent to child through a broken gene. In MLD, the body can't properly make the enzyme arylsulfatase A. This leads to a loss of myelin — the special coating that protects the body's nerves. Without enough myelin, the nerves stop working right.

    DA: 16 PA: 46 MOZ Rank: 80

  • MLD — a Rare and Serious Progressive Disease

    mayoclinic.org

    https://newsnetwork.mayoclinic.org/discussion/mld-a-rare-and-serious-progressive-disease/

    WEBJul 30, 2010 · Metachromatic leukodystrophy (MLD) is an inherited disorder that affects the protective covering around nerve cells (myelin sheath), as well as the nerve fibers that the sheath insulates and protects. A rare, serious and …

    DA: 5 PA: 71 MOZ Rank: 14

  • Metachromatic Leukodystrophy - Symptoms, Causes, Treatment

    rarediseases.org

    https://rarediseases.org/rare-diseases/metachromatic-leukodystrophy/

    WEBMar 18, 2024 · Metachromatic leukodystrophy (MLD) is a rare hereditary disease characterized by accumulation of fats called sulfatides. This causes the destruction of the protective fatty layer (myelin sheath) surrounding the nerves in both the central nervous system and the peripheral nervous system.

    DA: 93 PA: 76 MOZ Rank: 9

  • Metachromatic Leukodystrophy (MLD) - United Leukodystrophy Foundation

    ulf.org

    https://ulf.org/leukodystrophies/metachromatic-leukodystrophy-mld/

    WEBMetachromatic Leukodystrophy (MLD) is inherited in an autosomal recessive manner, and is most commonly caused by a mutation in a gene called arylsulfatase A (ASA), also called sulfatide sulfatase. The protein produced by ASA is present in the lysosome, a compartment of the cell that specializes in general “cleanup” of the cell.

    DA: 50 PA: 83 MOZ Rank: 63

  • Metachromatic Leukodystrophy (MLD) | Be The Match

    bethematch.org

    https://bethematch.org/patients-and-families/about-transplant/blood-cancers-and-diseases-treated-by-transplant/metachromatic-leukodystrophy--mld-/

    WEBWhat is metachromatic leukodystrophy (MLD)? MLD is a disease you’re born with that affects metabolism. Metabolism is how the body breaks down food into energy. In MLD, the body is missing an important protein (enzyme) to break down fat-based substances. When the fat-based substances aren’t broken down, they build up and cause damage.

    DA: 87 PA: 42 MOZ Rank: 44