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    Ehlers-Danlos syndrome: A case report
    (1996) Tasdemir N.; Sarac A.J.; Tombul T.; Erdogan F.; Ataoglu S.; Cevik R.
    Ehlers-Danlos syndrome a rare disease, it is inherited as an autosomal dominant trait. Clinically the skin is hyperextensible, fragile and brittle and bruises easily. The joints are hyperextensible and can be pulled apart longitudinally to an abnormal degree. We presented a patient who was complaining from muscle pain, muscle weakness and especially hyperextensible metacorpophalangeal and interphalangeal joints. We described that he has been suffering from EDS type II which is a less severe form of EDS. Then we reviewed this rare syndrome from the literature.
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    EMG findings in cases of spinal stenosis
    (1996) Tasdemir N.; Sarac A.J.; Erdogan F.; Ataoglu S.; Uyar A.; Cevik R.; Bekler H.
    Spinal stenosis resulting from ligamentous and osseous factors often causes complex neurologic complications. In this study, 54 cases who were clinically diagnosed a spinal stenosis were selected. 30 cases who were exactly diagnosed as spinal stenosis were selected. 30 cases who were exactly diagnosed as spinal stenosis by computed tomography (CT) were included in the study. In the measurement of spinal stenosis, the method of Jones Thompson and the conventional techniques on the CT imaging were used. The rates of sensory and motor messages, F wave, H reflex responses in the bilateral lower extremities of the cases were measured by Phasis Esaote Biomedica EMG equipment. In favour of bilateral multisegmented neurologic paralysis positive spine, the potentials of fibrillation denervation were observed when the involving of L5 anterior nerve root in 75% of cases, of L4 anterior nerve root in 75% of cases, of L4 anterior nerve root in 40% of that, of S1 anterior nerve root in 65% of that.
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    Ophthalmic findings in patients with rheumatoid arthritis
    (1995) Karakas N.; Sarac J.; Erdogan F.; Senerkek E.; Ataoglu S.; Unlu M.K.
    Ophthalmic findings of 31 patients (22 female, 9 male, age range 16-58) with rheumatoid arthritis (RA) were evaluated. The incidence of ocular pathology was found 45.16%, 32.25% of patients had keratoconjunctivitis sicca, 6.45% had filamantary keratitis and 3.23% had nodular scleritis. The probability of ocular pathology was found to be higher in patients with longer duration of (RA). The mean duration of the disease in patients with ocular pathology (13.30+4.32) was significantly higher than the mean duration in patients without ocular pathology (7.29+3.31) (p<0.001).