• Mucolipidosis type IV - Genetics Home Reference

    ghr.nlm.nih.gov/condition/mucolipidosis-type-iv Mucolipidosis type IV is an inherited disorder characterized by delayed development and vision impairment that worsens over time. The severe form of the ...
  • Mucolipidosis Type IV: an Update

    www.ncbi.nlm.nih.gov/pmc/articles/PMC3205274 Mucolipidosis type IV (MLIV) is a neurodevelopmental as well as neurodegenerative disorder with severe psychomotor developmental delay, progressive visual impairment ...
  • Mucolipidosis type IV - Wikipedia, the free encyclopedia

    en.wikipedia.org/wiki/Mucolipidosis_type_IV Mucolipidosis type IV (ML IV or ML4) is an autosomal recessive lysosomal storage disorder. Individuals with the disorder have many symptoms including delayed ...
    • Mucolipidosis Type IV (ML4) - Jewish Genetic Disease

      mazornet.com/genetics/ML4.htm Information and Resources for all Jewish Genetic Diseases: Mucolipidosis Type IV (ML4)
    • mucolipidosis type iv, ML4

      ml4.org ML4 Foundation, originally known as CHARM (Children's Association for Research on Mucolipidosis), reaching out to families affected with this debilitating disorder.
    • Mucolipidoses Fact Sheet

      www.ninds.nih.gov/disorders/mucolipidoses/detail_mucolipidoses.htm Mucolipidoses Fact Sheet. See a list of all NINDS Disorders. Get Web page suited for printing Email this to a friend or colleague ... Mucolipidosis type IV ...
    • Mucolipidosis Type IV - Integrated Genetics - LabCorp

      www.labcorp.com/wps/wcm/connect/IntGeneticsLib/.../mucolipidosis+type+iv Mucolipidosis Type IV (MLIV) is an inherited disease characterized by poor growth, severe developmental delay, and progressive vision loss.
    • Mucolipidosis Type IV | Icahn School of Medicine

      icahn.mssm.edu/research/genomics/genetic-testing/catalog/mucolipidosis Test Description: Mucolipidosis type IV (MLIV) is a neurodegenerative lysosomal storage disorder that is inherited in an autosomal recessive manner.
    • Mucolipidosis Type IV - Center for Jewish Genetics

      www.jewishgenetics.org/mucolipidosis-iv-mliv Mucolipidosis IV (MLIV) was first described in 1974. It is part of a group known as genetic lysosomal storage diseases, in which cells can’t produce an enzyme which ...
    • Mucolipidosis II alpha/beta - Genetics Home Reference

      ghr.nlm.nih.gov/condition/mucolipidosis-ii-alpha-beta Mucolipidosis II alpha/beta (also known as I-cell disease) is a progressively debilitating disorder that affects many parts of the body. Most affected ...