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Biomedical subjects

T Ozgür

Publications and source records attributed to T Ozgür.

4 recordsLinked to original sources

Hypozincaemia in febrile convulsion.

UNLABELLED: To understand further the role role of trace elements in pathogenesis of febrile convulsions, serum zinc (Zn), copper (Cu), magnesium (Mg) and CSF An, Cu, Mg and protein levels were measured by spectrometry in patients with febrile convulsion (n = 19), bacterial meningitis (n = 9), viral CNS infection (n = 16) and in the control group (n = 10) which consisted of children with signs of meningeal irritation due to upper respiratory tract infection but normal CSF findings. Samples were obtained within 6 h after admission to hospital. Mean serum and CSF Zn levels in the febrile convulsion group were significantly lower than in the other groups (for serum Zn: 0.66 +/- 0.03 mg/1 vs 0.98 +/- 0.07 mg/1, 1.06 +/- 0.08 mg/1, 1.05 +/- 0.09 mg/1 P < 0.05; for CSF Zn: 22.96 +/- 1.62 micrograms/1 vs 75.47 +/- 6.9 micrograms/1, 50.32 +/- 5.235 micrograms/1, 39.85 +/- 2.81 micrograms/1 P < 0.05). A linear relationship was established between serum Zn and CSF Zn levels (P < 0.001). Mean CSF Zn, Cu and protein levels in the bacterial meningitis group were significantly higher than in the other groups (for CSF Cu 63.94 +/- 6.33 micrograms/1 vs 38.77 +/- 2.70 micrograms/1, 35.84 +/- 3.48 micrograms/1, 33.86 +/- 2.88 micrograms/1 P < 0.05; for CSF protein 0.80 +/- 0.12 g/1 vs 0.22 +/- 0.02 g/1, 0.53 +/- 0.08 g/1, 0.19 +/- 0.01 g/1 P < 0.05). In children with meningitis, the elevation of the mean CSF Zn and Cu levels may result from the breakdown of the blood-brain barrier and subsequent leakage of trace elements and protein from serum to CSF. There was no significant difference between the four groups in terms of mean serum Mg and mean CSF Mg levels. CONCLUSION: Serum and CSF Zn levels are decreased in children with febrile seizures. Zinc deprivation may play a role in the pathogenesis of febrile seizures.

Adolescent↗

Origin of the anterior spinal artery.

This investigation was designed to extend our present knowledge of the origin of the anterior spinal a. and is based on 80 brains of human cadavers. The anterior spinal a. is usually formed rostrally by the union of the anterior spinal branches from the intracranial segments of the vertebral aa. In this study, we observed three different locations of the origin of the anterior spinal a. Each type has different characteristics. A bilateral origin (type I) was present in 60 specimens (75%). This type could be further subdivided according to the caliber of the arteries, into the following subtypes: "balanced" (type Ia 42.5%), right-dominated (type Ib 17.5%), and left-dominated (type Ic 15%). A unilateral origin (type II) was found in 9 specimens (11.3%), and an origin in an intervertebral transverse anastomosis was demonstrated in 11 (13.8%). In all cases, the anterior spinal a. had an average caliber of 1.145 +/- 0.12 mm.

Adult↗

A case report: corpus callosum dysgenesis, microcephaly, infantile spasm, cleft lip-palate, exophthalmos and psychomotor retardation.

In this report, a case with corpus callosum dysgenesis, infantile spasm, microcephaly, psychomotor retardation, exophthalmos, cleft lip-palate and abnormal EEG findings is presented. His parents are first-degree relatives. We could not fully match the findings of our patient with the criteria of any syndrome published to date.

Agenesis of Corpus Callosum↗

Ectopic thoracic kidney.

A five-month-old female infant was hospitalized for bronchopneumonia. Ultrasonography and other studies demonstrated the presence of an ectopic thoracic kidney with normal anatomical structures.

Female↗