Results for curschmann steinert

curschmann steinert

Myotonic dystrophy Curschmann-Steinert. PubMed NCBI.
Morphologically we observed a lack of facial expression manifesting as a myopathic facies and a moderate cachexia. Neurological findings included muscle weakness and atrophy in the extremities as well as of the sternocleidomastoid and temporal muscles a slight dysarthrophony and gait disturbance.
w montreal dictionary: Curschmann Steinert disease myotonic dystrophy type 1 DM1: German-English translation.
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z. German-English Dictionary: Curschmann Steinert disease myotonic dystrophy type 1 DM1. Tabular list of translations always.
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Whonamedit dictionary of medical eponyms.
Curschmann: Über partielle Myotonie unter dem Bilde einer Beschäftigungsneurose und Lähmung. Berliner klinische Wochenschrift, 1905, 42: 1175-1185. Über familiäre atrophische Myotonie. Deutsche Zeitschrift für Nervenheilkunde, 1912, 45: 161-202. Gibb: Myotonia atrophica. Brain, Oxford, 1909, 32: 187-205. Steinert: Myopathologische Beiträge. Über das klinische und anatomische Bilde des Muskelschwunds des Myotoniker.
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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.
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Curschmann-steinert-disease dictionary definition curschmann-steinert-disease defined.
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Morbus curschmann steinert myotone dys Spanish Translator.
Log In Sign Up. morbus curschmann steinert myotone dystrophie typ 1 dm1. á é í ó ú ñ. Show more translations. Use the three translators to create the most accurate translation. Explore the translation word-by-word. Find similarities across all translators.
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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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