Preoteasa D
Clinica de Oftalmologie, Craiova.
Oftalmologia. 1993 Oct-Dec;37(4):326-31.
66-year-old female patient presents palpebral bilateral ptosis and external ophthalmoplegia with a progressive evolution. The clinical aspects are completed with the affectation of the sensitive and motor trigemen, with the masseter atrophy and bilateral trophic keratitis. The affectation of the facial and acoustic nerves was associated with bilateral perception surditate. The hereditary transmission was dominant, with incomplete penetration. The neurogenic pathogeny was sustained on the basis of the association of neurological multilesions with III, IV, V, VI, VII, VIII nerves, with progressive extension.
66岁女性患者出现双侧眼睑下垂和外眼肌麻痹，并呈进行性发展。临床症状还包括三叉神经感觉和运动功能受累，伴有咬肌萎缩和双侧营养性角膜炎。面神经和听神经受累伴有双侧听力减退。遗传方式为显性遗传，外显不全。神经源性病因基于III、IV、V、VI、VII、VIII神经的多处神经病变关联且呈进行性扩展而成立。
