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- Hereditary_inclusion_body_myopathy abstract "Hereditary inclusion body myopathies (HIBM) are a heterogeneous group of genetic disorders which have different symptoms. Generally, they are neuromuscular disorders characterized by muscle weakness developing in young adults. Hereditary inclusion body myopathies comprise both autosomal recessive and autosomal dominant muscle disorders that have a variable expression (phenotype) in individual patients, but all share similar structural features in the muscles. HIBMs are a group of muscle wasting disorders, which are uncommon in the general world population. One autosomal recessive form of HIBM is known as IBM2, which is a common genetic disorder amongst people of Iranian Jewish descent. IBM2 has also been identified in other minorities throughout the world, including people of Asian (Japanese and others), European, and South American origin, as well as Muslim patients in the Middle Eastern, Palestinian, and Iranian origin. In Japan and many East Asian countries, this disorder is known as Distal Myopathy with Rimmed Vacuoles (DMRV).IBM2 causes progressive muscle weakness and wasting. Muscle wasting usually starts around the age of 20 – 30 years, although young onset at 17 and old onset at 52 has been recorded. As such, it affects the most productive times of our lives. It can progress to marked disability within 10 – 15 years, confining many patients to the wheelchair. The weakness and severity can vary from person to person. In some, weakness in the legs is noticed first. In few others, the hands are weakened more rapidly than the legs. Weakness is progressive, which means the muscle become weaker over time. IBM2 does not seem to affect the brain, internal organs or sensation. The quadriceps are relatively spared, and remain strong until the late stages of disease, which is the reason IBM2 is often referred to as Quadriceps Sparing Myopathy (QSM).".
- Hereditary_inclusion_body_myopathy wikiPageExternalLink fordoctors:what_is_hibm.
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- Hereditary_inclusion_body_myopathy wikiPageID "2662397".
- Hereditary_inclusion_body_myopathy wikiPageLength "7982".
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- Hereditary_inclusion_body_myopathy wikiPageRevisionID "678912061".
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Alzheimers_disease.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Autosomal_dominant.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Autosomal_recessive.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Bethesda,_MD.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Bethesda,_Maryland.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Buccal_swab.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Category:Muscular_disorders.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Dominance_(genetics).
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Hereditary.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Heredity.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Heterogeneous.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Homogeneity_and_heterogeneity.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Inclusion_bodies.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Inclusion_body.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Inclusion_body_myositis.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Myopathy.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink National_Human_Genome_Research_Institute.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Palliative.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Palliative_care.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Phenotype.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Quadriceps.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Quadriceps_femoris_muscle.
- Hereditary_inclusion_body_myopathy wikiPageWikiLink Sialic_acid.
- Hereditary_inclusion_body_myopathy wikiPageWikiLinkText "Hereditary inclusion body myopathy".
- Hereditary_inclusion_body_myopathy wikiPageWikiLinkText "hereditary inclusion body myopathy".
- Hereditary_inclusion_body_myopathy hasPhotoCollection Hereditary_inclusion_body_myopathy.
- Hereditary_inclusion_body_myopathy wikiPageUsesTemplate Template:Citation_needed.
- Hereditary_inclusion_body_myopathy wikiPageUsesTemplate Template:Refimprove.
- Hereditary_inclusion_body_myopathy wikiPageUsesTemplate Template:Reflist.
- Hereditary_inclusion_body_myopathy subject Category:Muscular_disorders.
- Hereditary_inclusion_body_myopathy hypernym Group.
- Hereditary_inclusion_body_myopathy type Article.
- Hereditary_inclusion_body_myopathy type Band.
- Hereditary_inclusion_body_myopathy type Article.
- Hereditary_inclusion_body_myopathy type Disorder.
- Hereditary_inclusion_body_myopathy comment "Hereditary inclusion body myopathies (HIBM) are a heterogeneous group of genetic disorders which have different symptoms. Generally, they are neuromuscular disorders characterized by muscle weakness developing in young adults. Hereditary inclusion body myopathies comprise both autosomal recessive and autosomal dominant muscle disorders that have a variable expression (phenotype) in individual patients, but all share similar structural features in the muscles.".
- Hereditary_inclusion_body_myopathy label "Hereditary inclusion body myopathy".
- Hereditary_inclusion_body_myopathy sameAs m.07w6r1.
- Hereditary_inclusion_body_myopathy sameAs Q5737853.
- Hereditary_inclusion_body_myopathy sameAs Q5737853.
- Hereditary_inclusion_body_myopathy wasDerivedFrom Hereditary_inclusion_body_myopathy?oldid=678912061.
- Hereditary_inclusion_body_myopathy isPrimaryTopicOf Hereditary_inclusion_body_myopathy.