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Öğe 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.Öğe 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.Öğe Gingival metastase and intracerebral haemorrhage resulting from unsuspected choriocarcinoma: A case report(2010) Tasdemir M.S.; Aktas A.; Tasdemir N.; Nergiz Y.Gestational choriocarcinoma is a higly malignant epithelial tumour arising from the trophoblasts of any type of gestational event, most often a hydatidiform mole. Choriocarcinoma is for all practical purposes limited to reproductive age women but rare examples of choriocarcinoma in postmenoupausal women have been reported. In case of a 24- years- old was a female patient with left hemiparalysis. Biopsy that obtained from lower gingival ulcer indicated the availability of choriocarcinoma metastasis. Before putting her in our intensive care unit she suddenly became unconscious. Focally haemorrhagic fragile gingival tissue (grossly, 1× 1× 0.5 cm) was processed. In the formaline fixed, paraffin embedded and hematoxylin and eosin(H&E) stained slides, beneath the stratified squamous epithelia, there was tumoral infiltration. Tumor was consisted of abnormal cytotrophoblasts and syncytiotrophoblasts cells and diffuse intercerebral haemorrhage. In this report we presented a rare case of metastatic gingival choriocarcinoma and intracranial haemorrhage resulting from an unsuspected choriocarcinoma metastasis.Öğe Peripheral neuropathy after burn injury.(2013) Tamam Y.; Tamam C.; Tamam B.; Ustundag M.; Orak M.; Tasdemir N.Peripheral neuropathy is a well-documented disabling sequela of major burn injury. These lesions are associated with both thermal and electrical injuries that may be frequently undiagnosed or overlooked in clinical settings. The purpose of this study was to evaluate the prevalence of burn-related neuropathy in our database and to investigate the clinical correlates for both mononeuropathy and generalized peripheral polyneuropathy. Out of 648 burn patients, admitted to our clinic forty-seven burn patients with the diagnosis of peripheral neuropathy were evaluated retrospectively. The demographic and clinical data collected were gender, age, degree, site and percent surface area of burn, type of burn, and the results of electrodiagnostic examination, including electromyography and nerve conduction assessments and associated pathology if existed. Peripheral neuropathy is the most frequent disabling neuromuscular complication of burn, that may be undiagnosed or overlooked. In current study, peripheral neuropathy associated with burn all of our patients were identified by electrodiagnostic study. After treatment in Burn Unit, clinical and electrodiagnostic studies were applied. Motor and sensory distal latencies were prolonged and sensory nerve action potentials reduced in amplitude. The findings of our study have shown that polyneuropathies and axonal neuropathy were more frequent than mononeuropathy and demyelination.Öğe Progressive external ophthalmoplegia (PEO): Presentation of a mitochondrial myopathy accompanied by electron microscope(2010) Aktas A.; Tasdemir M.S.; Tasdemir N.; Nergiz Y.Kearns-Sayre syndrome is a mitochondrial disease, presenting findings before the age of 20 and characterized by chronic progressive external ophthalmoplegia and pigmentary retinal degeneration. It affects many organs, resulting in a very wide spectrum of complications. In this work, a 24-year-old female, whose complaints first started at the age of 12, showing progressing external ophthalmoplegia and diagnosed with Kearns-Sayre disease following mitochondrial changes in muscle electron microscope investigation was presented. Ways of diagnosing in mitochondrial diseases, especially those in children were tried to be evaluated.
