Congenital familial external ophthalmoplegia
Koraszewska-Matuszewska, B.; Samochowiec-Donocikowa, E.
Klinika Oczna 86(10): 427-428
1984
ISSN/ISBN: 0023-2157 PMID: 6535872 Document Number: 239106
A family fitting the criterion for congenital familial fibrosis has electromyographic and clinical evidence of co-contraction. Forced ductions were negative in one patient. Muscle fibrosis in this family is thought to be secondary to the innervational anomaly akin to Duane's syndrome rather than a primary myogenic etiology. The evidence of a brainstem etiology makes classification as an ophthalmoplegia seem more appropriate.
Document emailed within 1 workday
Related Documents
Metz, H.S.; Meshel, L. 1974: Ocular saccades in progressive external ophthalmoplegia Annals of Ophthalmology 6(6): 623-628Inose, M.; Higuchi, I. 2002: Autosomal recessive chronic progressive external ophthalmoplegia Nihon Rinsho. Japanese Journal of Clinical Medicine 60(Suppl 4): 455-457
Higuchi, I.; Nakagawa, M. 2002: Autosomal dominant chronic progressive external ophthalmoplegia Nihon Rinsho. Japanese Journal of Clinical Medicine 60(Suppl 4): 450-454
Rodríguez-Hernández, M.; Hirano, M.; Arrieta, T.; Lestayo, Z.; Estrada, R.; Santiesteban, R.; Guerra-Badía, R.; Galarraga, J.; Gutierres, J.; Hechevarría, E.; Andreu, A.; Montoya, J.; DiMauro, S. 2000: Molecular studies in Cuban patients with progressive external ophthalmoplegia Revista de Neurologia 30(11): 1001-1005
Kawashima, S.; Nishizawa, M. 1993: Multiple mitochondrial DNA deletions in chronic progressive external ophthalmoplegia (CPEO) Nihon Rinsho. Japanese Journal of Clinical Medicine 51(9): 2391-2395
Fujimoto, S.; Ueyama, H.; Mita, S.; Kumamoto, T.; Tsuda, T. 1998: A case of chronic progressive external ophthalmoplegia presenting as inflammatory myopathy Rinsho Shinkeigaku 38(3): 228-232
Donzeau, J.P.; Constans, R.; Conte, D.; Rochiccioli, P.; Bernadet, P.; Bounhoure, J.P.; Calazel, P. 1977: Progressive external ophthalmoplegia and disorders of ventricular conduction. Apropos of 3 recent cases Archives des Maladies du Coeur et des Vaisseaux 70(8): 875-882
Lee, C.C.; Ko, Y.M.; Chen, S.S. 1992: Chronic progressive external ophthalmoplegia with NADH-CoQ reductase deficiency: report of a case Zhonghua Yi Xue Za Zhi 50(1): 77-82
Cohen, J.M.; Waiss, B. 1997: Combination ptosis crutch and moisture chamber for management of progressive external ophthalmoplegia Journal of the American Optometric Association 68(10): 663-667
Piccolo, G.; Cosi, V.; Poloni, M.; Moglia, A.; Marchetti, C.; Scelsi, R. 1982: Chronic progressive external ophthalmoplegia. Clinical, electrophysiological, histochemical and ultrastructural studies of 14 cases Schweizer Archiv für Neurologie Neurochirurgie und Psychiatrie 131(2): 161-174
Nakagawa, M.; Tokimura, M.; Kuriyama, M.; Higuchi, I.; Osame, M. 1991: Chronic progressive external ophthalmoplegia (CPEO); mitochondrial DNA deletion, brain MRi and electrophysiological studies Rinsho Shinkeigaku 31(9): 981-986
Boltshauser, E.; Jerusalem, F.; Niemeyer, G.; Huber, C. 1977: Kearns syndrome. Progressive external ophthalmoplegia, retinal pigment degeneration and heart conduction disorders Schweizerische Medizinische Wochenschrift 107(50): 1880-1888
Keiner, S.; Bootz, F. 1997: Ophthalmoplegia. Ophthalmoplegia in sphenoid sinus metastasis of a laryngeal carcinoma Hno 45(4): 238-239
Herranz Fernández, J.L.; Moreno Belzue, C.; Arce García, J.L.; Arteaga Manjón-Cabeza, R. 1992: Congenital familial hemiparesis and familial porencephaly Anales Espanoles de Pediatria 37(5): 431-433
Szabó, L.; Pap, V.; Almos, S.; Méhes, K. 1972: Congenital and familial occurrence of too large parietal apertures, congenital ptosis and typical facial expression Padiatrie und Grenzgebiete 11(1): 67-73
Beckmann, R.; Schmidt, D.; Ketelsen, U.P.; Schurmann-Bierl, K. 1978: Chronic progressive ocular muscular dystrophy v. Graefe. Chronic progressive external ophthalmoplegia (CPEO). Review of the literature based on 294 cases Die Medizinische Welt 29(25): 1030-1035
Wiedemann, H.R.; Dibbern, H. 1980: Congenital cutis laxa syndrome (Dermatochlasis connata). a familial syndrome with congenital loose skin and corresponding "aged look" in possible combination with more or less numerous further complications Die Medizinische Welt 31(13): 484
Kitazawa, K.; Yuki, N. 1995: Guillain-Barré syndrome associated with external ophthalmoplegia, consciousness disturbance, and extensor plantar responses: an overlap between Guillain-Barré syndrome and Bickerstaff's brainstem encephalitis Rinsho Shinkeigaku 35(6): 626-632
Soudek, K.; Randa, V.; Danĕk, J. 1987: Congenital familial adenomatosis Rozhledy V Chirurgii: Mesicnik Ceskoslovenske Chirurgicke Spolecnosti 66(4): 269-277
Scoppetta, C.; Lovaste, M.G.; Tonali, P.; Vaccario, M.L. 1977: Congenital familial myasthenia Acta Neurologica 32(6): 709-718