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Results 1 - 6 of 6 for Laminopathy
  1. LMNB1 gene 
    The LMNB1 gene provides instructions for making the lamin B1 protein. Lamin B1 is a structural protein called an intermediate filament protein. Intermediate ...
    https://medlineplus.gov/genetics/gene/lmnb1 - Genetics
  2. Autosomal dominant leukodystrophy with autonomic disease 
    Autosomal dominant leukodystrophy with autonomic disease (ADLD) is one of a group of genetic disorders called leukodystrophies. Leukodystrophies are characterized ...
    https://medlineplus.gov/...ant-leukodystrophy-with-autonomic-disease - Genetics
  3. Hutchinson-Gilford progeria syndrome 
    Hutchinson-Gilford progeria syndrome is a genetic condition characterized by the dramatic, rapid appearance of aging beginning in childhood. Affected children typically ...
    https://medlineplus.gov/.../hutchinson-gilford-progeria-syndrome - Genetics
  4. Lonafarnib 
    ... also used to treat certain processing-deficient progeroid laminopathies (PDPL; inherited disorders that cause certain proteins to ...
    https://medlineplus.gov/druginfo/meds/a622036.html - Drugs and Supplements
  5. LMNA gene 
    ... from mutations in lamin proteins are known as laminopathies. These disorders often have overlapping signs and symptoms, ... the same LMNA mutation. Researchers suspect that some laminopathies represent variants of a single condition instead of ...
    https://medlineplus.gov/genetics/gene/lmna - Genetics
  6. Emery-Dreifuss muscular dystrophy 
    ... G, Quijano-Roy S. Emery-Dreifuss muscular dystrophy, laminopathies, and other nuclear envelopathies. Handb Clin Neurol. 2013; ... A. Emery-Dreifuss muscular dystrophy: the most recognizable laminopathy. Folia Neuropathol. 2016;54(1):1-8. doi: ...
    https://medlineplus.gov/.../emery-dreifuss-muscular-dystrophy - Genetics