[Myoadenylate deaminase deficiency among patients with myasthenia gravis--preliminary results of exercise]

Autor: Małgorzata, Bilińska, Zygmunt, Chodorowski, Walenty, Nyka, Wiesława, Nyka, Iwona, Rybakowska, Ryszard, Smoleński, Krystian, Kaletha
Rok vydání: 2004
Předmět:
Zdroj: Przeglad lekarski. 60(11)
ISSN: 0033-2240
Popis: Myasthenia Gravis (MG) is a primary disorder of neuromuscular transmission, and patients suffering from this disease manifest specific, progressive weakness of several groups of skeletal muscles. Myoadenylate deaminase deficiency (MADD) is an inborn disease of skeletal muscles, the clinical symptoms of which may mimic symptoms observed in MG. Preliminary results of studies presented in this paper suggest that simultaneous occurrence of MG and MADD may modify energetic metabolism of skeletal muscle.
Databáze: OpenAIRE