19 research outputs found

    Diagnosis and treatment process of comorbid bipolar disorder in a patient diagnosed with autism: Case report

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    Depression is one of the main psychiatric comorbidity reported in individuals with autism spectrum disorder (ASD). However, some cases of bipolar disorder accompanying ASD have been reported. In the past, there was a tendency to attribute all psychiatric problems in autistic children and adults to autism itself. Nowadays, there is not only an increase in the number of studies on other medical conditions especially neurological conditions in ASD but also there is an increasing effort in defining the comorbide psychiatric disorders. Comorbid psychiatric conditions can make disease management difficult in cases of autism. The precise and reliable diagnosis of psychiatric disorders accompanying children and adolescents with autism is of great importance. More specific treatment options are possible when problematic behaviors are accepted only as a manifestation of comorbid psychiatric disorder from isolated behavior. In this case report, we aimed to present the diagnosis and management of an adolescent autism diagnosed patient and comorbid bipolar disorder

    The effects of docosahexaenoic acid on glial derived neurotrophic factor and neurturin in bilateral rat model of Parkinson's disease.

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    Parkinson's disease (PD) is the second most common neurodegenerative disorder marked by cell death in the Substantia nigra (SN). Docosahexaenoic acid (DHA) is the major polyunsaturated fatty acid (PUFA) in the phospholipid fraction of the brain and is required for normal cellular function. Glial cell line derived neurotrophic factor (GDNF) and neurturin (NTN) are very potent trophic factors for PD. The aim of the study was to evaluate the neuroprotective effects of GDNF and NTN by investigating their immunostaining levels after administration of DHA in a model of PD. For this reason we hypothesized that DHA administration of PD might alter GDNF, NTN expression in SN. MPTP neurotoxin that induces dopaminergic neurodegeneration was used to create the experimental Parkinsonism model. Rats were divided into; control, DHA-treated (DHA), MPTP-induced (MPTP), MPTP-induced+DHA-treated (MPTP+DHA) groups. Dopaminergic neuron numbers were clearly decreased in MPTP, but showed an increase in MPTP+DHA group. As a result of this, DHA administration protected dopaminergic neurons as shown by tyrosine hydroxylase immunohistochemistry. In the MPTP+DHA group, GDNF, NTN immunoreactions in dopaminergic neurons were higher than that of the MPTP group. In conclusion, the characterization of GDNF and NTN will certainly help elucidate the mechanism of DHA action, and lead to better strategies for the use of DHA to treat neurodegenerative diseases

    Volume CXIV, Number 4, November 7, 1996

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    Objective: Turner syndrome (TS) is a chromosomal disorder caused by complete or partial X chromosome monosomy that manifests various clinical features depending on the karyotype and on the genetic background of affected girls. This study aimed to systematically investigate the key clinical features of TS in relationship to karyotype in a large pediatric Turkish patient population.Methods: Our retrospective study included 842 karyotype-proven TS patients aged 0-18 years who were evaluated in 35 different centers in Turkey in the years 2013-2014.Results: The most common karyotype was 45,X (50.7%), followed by 45,X/46,XX (10.8%), 46,X,i(Xq) (10.1%) and 45,X/46,X,i(Xq) (9.5%). Mean age at diagnosis was 10.2±4.4 years. The most common presenting complaints were short stature and delayed puberty. Among patients diagnosed before age one year, the ratio of karyotype 45,X was significantly higher than that of other karyotype groups. Cardiac defects (bicuspid aortic valve, coarctation of the aorta and aortic stenosis) were the most common congenital anomalies, occurring in 25% of the TS cases. This was followed by urinary system anomalies (horseshoe kidney, double collector duct system and renal rotation) detected in 16.3%. Hashimoto's thyroiditis was found in 11.1% of patients, gastrointestinal abnormalities in 8.9%, ear nose and throat problems in 22.6%, dermatologic problems in 21.8% and osteoporosis in 15.3%. Learning difficulties and/or psychosocial problems were encountered in 39.1%. Insulin resistance and impaired fasting glucose were detected in 3.4% and 2.2%, respectively. Dyslipidemia prevalence was 11.4%.Conclusion: This comprehensive study systematically evaluated the largest group of karyotype-proven TS girls to date. The karyotype distribution, congenital anomaly and comorbidity profile closely parallel that from other countries and support the need for close medical surveillance of these complex patients throughout their lifespa

    Transition Probabilities of Neutral Scandium

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    WOS:000344602200021The electric dipole transition probabilities and the oscillator strengths of neutral scandium have been calculated using the quantum defect orbital theory and the Cowan code for the 3d4s(2)-3d4s4p, 3d(2)4s-3d(2)4p, and 3d4s(2)-4s(2)4p transitions. In addition, a parametric analysis of the fine structure for the 3d4s(2) configuration of even parity is performed using Cowan code. The transition probabilities and the oscillator strengths obtained in this work are mostly in agreement with the data obtained from different theoretical works given in the literature. Moreover, transition probabilities for 24 levels of neutral scandium are given for the first time

    The effects of docosahexaenoic acid on glial derived neurotrophic factor and neurturin in bilateral rat model of Parkinson's disease.

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    Parkinson's disease (PD) is the second most common neurodegenerative disorder marked by cell death in the Substantia nigra (SN). Docosahexaenoic acid (DHA) is the major polyunsaturated fatty acid (PUFA) in the phospholipid fraction of the brain and is required for normal cellular function. Glial cell line derived neurotrophic factor (GDNF) and neurturin (NTN) are very potent trophic factors for PD. The aim of the study was to evaluate the neuroprotective effects of GDNF and NTN by investigating their immunostaining levels after administration of DHA in a model of PD. For this reason we hypothesized that DHA administration of PD might alter GDNF, NTN expression in SN. MPTP neurotoxin that induces dopaminergic neurodegeneration was used to create the experimental Parkinsonism model. Rats were divided into; control, DHA-treated (DHA), MPTP-induced (MPTP), MPTP-induced+DHA-treated (MPTP+DHA) groups. Dopaminergic neuron numbers were clearly decreased in MPTP, but showed an increase in MPTP+DHA group. As a result of this, DHA administration protected dopaminergic neurons as shown by tyrosine hydroxylase immunohistochemistry. In the MPTP+DHA group, GDNF, NTN immunoreactions in dopaminergic neurons were higher than that of the MPTP group. In conclusion, the characterization of GDNF and NTN will certainly help elucidate the mechanism of DHA action, and lead to better strategies for the use of DHA to treat neurodegenerative diseases

    Shaken Baby Syndrome: Case Report

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    WOS: 000314145000048Shaken baby syndrome (SBS) is a serious type of physical abuse characterized by subdural hematoma and retinal hemorrhage. This syndrome is frequently seen in children younger than 2 years of age. Most of the time it results in death or severe neurological damage. In these cases, external visible injuries are generally absent; often there no history of shaking or trauma. Clinical symptoms and findings are nonspecific. Therefore, most of the cases are missed when SBS is not considered in the differential diagnosis. In this article, we reported two SBS cases admitted to our hospital with a history of head trauma and convulsions, resulting in death in one case

    Poster Presentations

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