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 (MLIV) is a neurodevelopmental as well as neurodegenerative disorder with severe psychomotor developmental delay, progressive visual impairment ...
Mucolipidosis type IV (ML IV or ML4) is an autosomal recessive lysosomal storage disorder. Individuals with the disorder have many symptoms including delayed ...
Information and Resources for all Jewish Genetic Diseases: Mucolipidosis Type IV (ML4)
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. 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 (MLIV) is an inherited disease characterized by poor growth, severe developmental delay, and progressive vision loss.
Test Description: Mucolipidosis type IV (MLIV) is a neurodegenerative lysosomal storage disorder that is inherited in an autosomal recessive manner.
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 (also known as I-cell disease) is a progressively debilitating disorder that affects many parts of the body. Most affected ...