Charcot-Marie-Tooth (CMT) hastalığı, periferik nervöz sistemin en sık görülen dejeneratif bir hastalığıdır. Genellikle otozomal dominant olarak kalıtılır. Tanı, aile öyküsü ve fizik muayenedeki karakteristik bulgulara dayanır. Kraniyal sinir tutulumu nadir görülür. Bu yazıda, bilateral altıncı sinir tutulumu olan CMT hastalığının sunulması amaçlandı.
Charcot-Marie-Tooth (CMT) disease is the most common hereditary degenerative disorder of the peripheral nervous system. It is generally inherited in an autosomal dominant pattern. Clinical diagnosis is based on family history and characteristic findings on physical examination. Cranial nerve involvement is rare. In this paper, it is aimed to report bilateral abducens nerve palsy involvement in CMT disease.
Other ID | JA52TF72EP |
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Journal Section | Case Reports |
Authors | |
Publication Date | March 1, 2017 |
Submission Date | March 1, 2017 |
Published in Issue | Year 2017Volume: 56 Issue: 1 |