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myozitída s inklúznymi telieskami

Č. záznamu	d018979
Dátum	06.06.2025
Typ	M
Tematický termín	myozitída s inklúznymi telieskami
Iný termín	Angličtina (Pseudonym) Inclusion Body Myositis Angličtina (Pseudonym) Myopathy, Inclusion Body, Sporadic Slovenčina (Pseudonym) myopatia sporadická, s inklúznymi telieskami
MDT	C05.651.594.600C10.668.491.562.500
Poznámka	Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10)

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