English
| dc.contributor.author | Çelebisoy, N | |
| dc.contributor.author | Orujov, A | |
| dc.contributor.author | Balayeva, F | |
| dc.contributor.author | Özdemir, HN | |
| dc.contributor.author | Ak, AK | |
| dc.contributor.author | Gökçay, F | |
| dc.date.accessioned | 2024-07-18T11:57:24Z | |
| dc.date.available | 2024-07-18T11:57:24Z | |
| dc.description.abstract | SPRINGER HEIDELBERG | |
| dc.identifier.issn | 2240-2993 | |
| dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/7065 | |
| dc.language.iso | Article | |
| dc.publisher | 0300-9009 | |
| dc.subject | Background Ocular myasthenia gravis (OMG) constitutes 15% of all myasthenia gravis patients. MethodsOne hundred eight patients with OMG followed-up for over 36 months were retrospectively evaluated regarding factors associated with remission. Demographic features, neuro-ophthalmologic findings at onset, acetylcholine receptor (AChR Ab) and muscle-specifc tyrosine kinase antibodies (MuSK Ab), thymic status, single fiber electromyography (SFEMG) results were the variables considered. ResultsMedian age of disease onset was 57 years (range 18-82 years). Clinical features at onset was isolated ptosis in 55 (50.9%) and isolated diplopia in 33 (30.6%) patients. Combined ptosis and diplopia were present in 20 (18.5%) patients. Among 75 patients with ptosis, it was unilateral in 65 (86.7%) and bilateral in 10 (13.3%). AChR Abs were found in 66 (61.1%) and MuSK Abs in 2 (1.9%) patients. SFEMG abnormality was detected in 74 (68.5%) patients. Thymoma was present in 16 (14.8%) and thymic hyperplasia in 6 (5.6%) patients. Forty-one patients (37.9%) had been treated with pyridostigmine alone. Sixty-seven (62%) patients were given immunosupressive drugs. In 53 (49.1%) prednisone was used and in 14 (12.9%) patients it was combined with azathioprine. Thymectomy was performed in all 16 patients with thymoma. Complete stable remission (CSR) was achieved in 49 (45.4%) patients. Fifty-nine (54.6%) patients had reached minimal manifestation (MM) status; 32 (29.6%) having a status of MM-1 and 27 (25%) a status of MM-3. ConclusionsThe presence of AchR Abs (p = 0.034) and an abnormal SFEMG (p = 0.006) at onset as increased risk factors for the presence of ongoing signs necessitating medical treatment. | |
| dc.title | English | |
| dc.type | ACETYLCHOLINE-RECEPTOR | |
| dc.type | GUIDELINES | |
| dc.type | DIAGNOSIS | |
| dc.type | ANTIBODY |