Soyağacı görüntüleme

In addition, soyağacı görüntüleme records of patients who had been admitted to our pediatric neurology outpatient clinic between January and May were examined, soyağacı görüntüleme, retrospectively, and 21 patients fitting to our study criteria were included in the study, prospectively. The patients were examined for demographical data, complaints on admission, perinatal events, consanguinity between parents and presence of similar disease in the family, convulsion and mental and motor development.

The patients were examined for demographical data, complaints on admission, perinatal events, consanguinity between parents and presence of similar disease in the family, convulsion and motor-mental development. Detailed physical and neurological examination were perfomed in all patients. A pedigree for each patient has been established in all patients. In order to detect etiological or other accompanying abnornalities, all patients have been tested for hematological and biochemical laboratory tests, serum vitamin B12 and folate levels, tandem-mass spectrometry, metabolic disease screening, brain magnetic resonance imaging, electroencephalography, visual evoked potential, brainstem auditory evoked response and intelligence test. If necessary, further investigations such as serum markers for TORCH group infections, organic acid profile in urine, computerized cranial tomography and abdominal ultrasonography have been performed.

Soyağacı görüntüleme

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Eleven patients had soyağacı görüntüleme epilepsy, two patients had partial epilepsy and the other two patients had a partial epilepsy with secondary generalization. Eight

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Soyağacı görüntüleme

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Exitus history was present in three patients and abortus history was present in the other three patients. In the 3rd group, while 17 patients had both epilepsy and MMR, two patients had epilepsy and mental retardation. A pedigree for each patient has been established in all patients. Eight There were three In the analysis of patients? Key Words: Child, pedigree, familial epilepsy, intellectual disability, motor retardation. A 1st and 2nd degree consanguineous marriage histories were present in nine First cousins once removed marriage was present in two Sixteen

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The patients were examined for demographical data, complaints on admission, perinatal events, consanguinity between parents and presence of similar disease in the family, convulsion and mental and motor development. In this study, 20 In addition, the records of patients who had been admitted to our pediatric neurology outpatient clinic between January and May were examined, retrospectively, and 21 patients fitting to our study criteria were included in the study, prospectively. In this study, 22 If necessary, further investigations such as serum markers for TORCH group infections, organic acid profile in urine, computerized cranial tomography and abdominal ultrasonography have been performed. First cousin marriage was present in seven Exitus history was present in three patients and abortus history was present in the other three patients. There were 15 patients in group 2. In order to detect etiological or other accompanying abnornalities, all patients have been tested for hematological and biochemical laboratory tests, serum vitamin B12 and folate levels, tandem-mass spectrometry, metabolic disease screening, brain magnetic resonance imaging, electroencephalography, visual evoked potential, brainstem auditory evoked response and intelligence test. Exitus history was present in two patients, abortus history was present in three patients and both of exitus and abortus history was present in two patients. The mean age on admission was 6.