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myotonia/karijes

Veza se sprema u međuspremnik
ČlanciKlinička ispitivanjaPatenti
3 rezultatima

Steinert syndrome and repercussions in dental medicine.

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Prijava Registriraj se
Steinert syndrome, also called myotonic dystrophy type 1, is a genetic disorder with autosomal dominant transmission characterized by myotonia and a multisystemic clinical picture that affects several tissues of the human body. The most common systemic phenotypes are: muscular, cardiac, respiratory,

On oral health in children and adults with myotonic dystrophy.

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Prijava Registriraj se
BACKGROUND Myotonic Dystrophy type 1 (DM1) is a hereditary neuromuscular multisystem disease with varying clinical expressions and severity. The prevalence worldwide is 5-20/100 000. It is characterized by progressive muscular waste and myotonia. Facial weakness is one of the earliest and most
OBJECTIVE Although chloride channels are involved in several physiological processes and acquired diseases, the availability of compounds selectively targeting CLC proteins is limited. ClC-1 channels are responsible for sarcolemma repolarization after an action potential in skeletal muscle and have
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