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curschmann steinert

Progressieve spierdystrofie.
Muscle weakness and impaired movement in legs, hands and arms, and restricted fine motor skills manual skills. Some diseased muscles appear particularly strong because the typical tissue composition of the perishing muscle fibres is embedded in fatty and connective tissue.
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Maculopathy in Curschmann-Steinert myotonic dystrophy. PubMed NCBI.
Because of remarkable deformations of jaw and teeth, a high hairline and an uncertain step we arranged a neurological consultation. Clinical observation together with myotonic activities in electromyography and diffuse lesions in the cerebral medular corpus shown in MRT led to the diagnosis of myotonic dystrophy Curschmann Steinert syndrome.
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Multiple basaliomas in Curschmann-Steinert myotonia atrophica Abstract Europe PMC.
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Curschmann-Steinert disease Wiktionary.
Definition from Wiktionary, the free dictionary. Jump to navigation Jump to search. Curschmann Steinert disease uncountable. A form of myotonic dystrophy type 1. English uncountable nouns. English words not following the I before E except after C rule. Not logged in.
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Myotonic dystrophy Curschmann-Steinert Request PDF.
Because of remarkable deformations of jaw and teeth, a high hairline and an uncertain step we arranged a neurological consultation. Clinical observation together with myotonic activities in electromyography and diffuse lesions in the cerebral medular corpus shown in MRT led to the diagnosis of myotonic dystrophy Curschmann Steinert syndrome.
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EEG observations in dystrophia myotonica Curschmann-Steinert.
ERG and EEG changes in Steinert myotonic dystrophy. January 1970 Electroencephalography and Clinical Neurophysiology. The concept of attention and the EEG alpha rhythm. March 1968 Electroencephalography and Clinical Neurophysiology. The electroencephalogram in Alzheimer-type dementa: A sequential study correlating the electroenceph.
Späte Diagnose einer myotonen Dystrophie Curschmann-Steinert bei einer Patientin mit Dilatativer Kardiomyopathie und ihrem Sohn Request PDF.
A 52-year-old man with myotonic dystrophy and first degree atrioventricular block, right bundle branch block and left anterior hemiblock was shown by echocardiographic examination to have hypertrophy of the posterior segment of the septum and of the anterior left ventricular wall.
Curschmann-Steinert disease definition of Curschmann-Steinert disease by Medical dictionary.
Steinhert, Hans, German physician, 1875. Curschmann-Batten-Steinert syndrome see under Curschmann. Steinert disease a chronic, slowly progressing disease marked by atrophy of the muscles, failing vision, lenticular opacities, ptosis, slurred speech, and general muscular weakness. Synonyms: myotonic dystrophy. Steinert myotonic dystrophy.
Myotonic dystrophy Curschmann-Steinert. PubMed NCBI.
Electromyography EMG showed signs of a myopathic process in the proximal muscles of the lower extremities right and left vastus medialis muscle. Although no typical myotonic discharges were recorded in the EMG, molecular testing confirmed the clinical suspicion of myotonic dystrophy type Curschmann-Steinert.
Multiple pigmentierte Basaliome im Capillitium bei Myotonia dystrophia Curschmann-Steinert Bestätigung einer seltenen Symptomenkonstellation SpringerLink.
Bereits 1986 haben Stieler und Plewig auf das gemeinsame Vorkommen von multiplen Basaliomen und Myotonia dystrophica Curschmann-Steinert hingewiesen. Möglicherweise besteht eine genetisch fixierte, erhöhte Disposition zu verschiedenen multiplen Hauttumoren mit follikulärem Ursprung, denn auch multiple Pilomatrixome werden bei der Myotonia dystrophica Curschmann-Steinert gefunden.
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