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Öğe Abortion and Protection of Fetal Life(Georg Thieme Verlag Kg, 2022) Caksen, Huseyin[Abstract Not Availabe]Öğe A case of Human Parechovirus Infection in an Infant with Meningitis(Aves Yayincilik, Ibrahim Kara, 2021) Tokak, Semih; Ozdemir, Mehmet; Gulseren, Yasemin Derya; Caksen, HuseyinHuman parechovirus is a potentially serious viral infection in neonates and infant and its importance increasing by years. In young infants, the typical clinical presentation includes fever, severe irritability, and rash, often leading to descriptions of hot, red, angry babies. We report a case of a 43-day-old girl with a fever that required hospitalization and in which human parechovirus was identified in the cerebrospinal fluid. Blood, urine, and cerebrospinal fluid bacterial cultures of the patient were negative and the patient has improved.Öğe Case of twin achondroplasia and autism coexistence and literature review(Lippincott Williams & Wilkins, 2023) Bilgec, Nagehan; Balasar, Ozgur; Uzun, Necati; Pekcan, Sevgi; Bedel, Fayize Maden; Caksen, HuseyinAchondroplasia and autism spectrum disorder (ASD) are two genetically based disorders. The coexistence of autism with chromosomal abnormalities such as Down syndrome, monogenic syndromes such as tuberous sclerosis, Fragile X, and Rett syndrome, and microdeletion syndromes such as Phelan-McDermid syndrome helps to shed light on the genetic basis of autism spectrum disorder. The association between ASD and achondroplasia has been reported twice in the literature. In this article, we report Turkish patients who were born as identical twins from IVF pregnancy of 34 and 36-year-old parents, clinically and molecularly diagnosed with achondroplasia, and diagnosed with ASD at the age of 39 months. Our case is the first twin patient with the coexistence of achondroplasia and autism. We discuss environmental and genetic factors contributing to the development of ASD.Copyright (c) 2023 Wolters Kluwer Health, Inc. All rights reserved.Öğe Children with Migraine and Those with Tension-Type Headache for Psychiatric Symptoms and Quality of Life (vol 19, pg 14, 2021)(Georg Thieme Verlag Kg, 2021) Acikel, Sadettin Burak; Bilgic, Ayhan; Derin, Hatice; Eroglu, Arzu; Akca, Omer Faruk; Caksen, Huseyin[Abstract Not Availabe]Öğe Closing the Gap between Pediatric and Adult Care: Establishing Proper Transition Care(Georg Thieme Verlag Kg, 2020) Kasper, Ekkehard M.; Caksen, Huseyin[Abstract Not Availabe]Öğe Comparison of Children with Migraine and Those with Tension-Type Headache for Psychiatric Symptoms and Quality of Life(Georg Thieme Verlag Kg, 2021) Acikel, Burak Sadettin; Bilgic, Ayhan; Derin, Hatice; Eroglu, Arzu; Akca, Omer Faruk; Caksen, HuseyinThis study compared the severity of depression, anxiety, somatization, anxiety sensitivity, sleep disturbances, and quality of life (QoL) among children with migraine, children with tension-type headache (TTH), and healthy children. A total of 37 children with migraine, 22 with TTH, and a healthy control group (n =35) participated in this study. Children with migraine exhibited higher depression and somatization and lower QoL scores than those in the control group. General sleep disturbances, bedtime resistance, sleep onset delay, sleep duration, sleep anxiety, night wakings, sleep-disordered breathing, and daytime sleepiness scores were also higher in those in the migraine group than in the control group. Regression models indicated that the severity of headache and depression scores significantly affected the QoLs of children with headache disorder as a whole. Migraine is associated with depression, somatization, sleep disturbances, and poor QoL, whereas TTH is associated with only sleep disturbances in childhood. The impact of headache on the QoL occurs mainly through the headache-specific and psychiatric factors.Öğe Comparison of Clinical and Neuroimaging Characteristics of Congenital and Possible Congenital Cytomegalovirus Infected Infants: A Retrospective Study(Georg Thieme Verlag Kg, 2019) Tarakci, Nuriye; Bulut, Cahide; Caksen, Huseyin; Ors, RahmiBackground To evaluate clinical and neurodevelopmental outcomes and neuroimaging results of patients diagnosed with congenital cytomegalovirus (cCMV) infection and those diagnosed with possible congenital CMV (possible cCMV) infection. Methods From January 2014 to January 2016, 24 patients were diagnosed with congenital CMV infection. Clinical and neuroimaging results of these patients were examined from their medical records. Results Of the 24 patients, 6 were diagnosed with cCMV, whereas 18 patients were diagnosed with possible cCMV. Petechia was the most common symptom observed in patients with cCMV infection, whereas microcephaly was more common in patients with possible cCMV. Of the 24 patients, 5 (20.8%) showed normal neuroimaging characteristics. The most commonly encountered abnormal findings in brain magnetic resonance imaging were hypoplasia of corpus callosum (16.7%) and hydrocephalous (16.7%). All of the patients had poor neurodevelopmental outcomes. Conclusions Early diagnosis of asymptomatic cCMV infection is difficult. This study suggests that possible cCMV infections are more prevalent compared with cCMV infections, and delays in diagnosis occur due to not keeping suspicion of CMV infection in early phase. Clinicians should consider long-term neurodevelopmental sequelae of cCMV and possible cCMV infections and remember to screen congenital CMV infection in suspected individuals.Öğe A congenital cranial dysinnervation disorder: Mobius' syndrome(Aves, 2017) Albayrak, Hatice Mutlu; Tarakci, Nuriye; Altunhan, Huseyin; Ors, Rahmi; Caksen, HuseyinMbius' syndrome, also known as Mbius' sequence, is a nonprogressive cranial dysinnervation disorder characterized by congenital facial and abducens nerve paralysis. Here, we report a 5-day-old girl who was conceived after in vitro fertilization with poor suck and facial paralysis. She had bilaterally ptosis and lateral gaze limitation, left-sided deviation of the tongue, dysmorphic face, hypoplastic fingers and finger nails on the left hand, and was diagnosed as having Mbius' syndrome. Involvement of other cranial nerves such as three, four, five, nine, 9 and 12, and limb malformations may accompany this syndrome. However, several factors have been proposed for the etiology, some rare cases have also been reported with artificial reproductive technologies. Feeding difficulties and aspiration are the main problems encountered in infancy. The other cranial nerves should be examined further in newborns who present with congenital facial palsy, and other cranial dysinnervation disorders should be considered in the differential diagnosis.Öğe Considerations for health professionals supporting parents of children with chronic or fatal diseases(Soc Argentina Pediatria, 2021) Caksen, Huseyin[Abstract Not Availabe]Öğe Coronavirus Disease 2019-Related Fulminant Idiopathic Intracranial Hypertension(Georg Thieme Verlag Kg, 2023) Caliskan, Burcu; Canbal, Abdullah; Guven, Ahmet Sami; Bitirgen, Gulfidan; Erdi, Mehmet Fatih; Caksen, HuseyinIdiopathic intracranial hypertension or pseudotumor cerebri syndrome (PTCS) is defined as an increase in intracranial pressure (ICP) without an identifiable and/or structural cause or abnormal cerebrospinal fluid content. The most common symptoms of PTCS include headache, vomiting, pulsatile tinnitus, blurred vision, and diplopia. In 2 to 3% of PTCS patients, severe and rapidly progressive vision loss may develop within 1 month since symptoms begin; this clinical condition is usually defined as fulminant idiopathic intracranial hypertension (FIIH). This study presented a patient admitted to the hospital with headache and blurred vision, who also had high severe acute respiratory syndrome coronavirus 2 infections total antibody level and was treated with a lumboperitoneal shunt due to medical treatment-resistant increased ICP. We also reviewed similar cases previously reported in the literature. To the best of our knowledge, no children affected with coronavirus 2019 related to FIIH and requiring surgical treatment have been yet reported in the literature.Öğe Correspondence: the importance of supplication for parents in the Neonatal Intensive Care Unit(Hygeia Press Corridori Marinella, 2021) Caksen, Huseyin[Abstract Not Availabe]Öğe Cortical Dysplasias, and Corpus Callosum and Posterior Fossa Abnormalities Correlation of Clinical Findings With Magnetic Resonance Imaging (MRI) Characteristics(Sage Publications Inc, 2014) Caksen, Huseyin; Kizilyildiz, Baran Serdar; Avcu, SerhatThis study examined clinical findings and magnetic resonance imaging (MRI) characteristics in 114 patients with cortical dysplasia and corpus callosum and posterior fossa abnormalities to determine the clinical findings with the extent of the lesions on MRI. The age of patients was between 1 day and 15 years. Group 1 included 74 patients with corpus callosum abnormalities and/or cortical dysplasias and group 2 included 40 patients with posterior fossa abnormalities, which were isolated and/or associated with cortical dysplasia and/or corpus callosum abnormalities. Although associated congenital abnormality apart from central nervous system abnormalities, syndrome, or systemic disorder were more common in group 2 than group 1 patients (P < .05), we did not find a difference between the groups for psychomotor retardation and epilepsy (P > .05).Öğe Death is a Bounty for Some Children With Terminal Cancer(Lippincott Williams & Wilkins, 2021) Caksen, Huseyin[Abstract Not Availabe]Öğe Dogs Bites in Children and a Spiritual View to Dogs(Georg Thieme Verlag Kg, 2022) Caksen, Huseyin[Abstract Not Availabe]Öğe The Effects of Quran Recitation on Sedation and Pain in Children(Georg Thieme Verlag Kg, 2023) Caksen, Huseyin[Abstract Not Availabe]Öğe Electrocardiographic ST elevation (mosque sign) without myocardial ischemia in an infant with tuberous sclerosis(Georg Thieme Verlag Kg, 2014) Alp, Hayrullah; Baysal, Tamer; Karaarslan, Sevim; Alpmar, Abdullah; Caksen, HuseyinRhabdomyomas, the most common primary cardiac tumors seen in infants and children, are often associated with tuberous sclerosis. However, these cardiac rhabdomyomas may cause hemodynamic disturbances and arrhythmias. In the present case, we demonstrated an infant with electrocardiographic ST elevation suggesting myocardial ischemia associated with multiple cardiac rhabdomyomas.Öğe Electronic Screen Exposure and Headache in Children(Wolters Kluwer Medknow Publications, 2021) Caksen, HuseyinHeadache represents the most common neurologic disorder in the general population including children and is increasingly being recognized as a major source of morbidity in youth related to missed school days and activities. Electronic screens are becoming increasingly important in the lives of preteens and teens. In this review, we discussed effects of electronic screens on primary headache in childhood to emphasize the importance of electronic screen exposure in children with headache. Using digital and social media can bring some benefits and risks for mental and physical health. Time spent on screen-based activities contributes to the chance of reporting general physical complaints, in particular, headache and backache during early adolescence. We suggest that all children with primary headache should be evaluated for abuse of electronic screens in neurology practice. We also think that restriction of electronic screen should be advised in children with migraine and tension type headache before initiation of pharmacotherapy. As online classes are a reality, use of electronic screen may be allowed for school age children up to 2 h/day with taking time away from digital media every 20 min for 20 sec. In conclusion, we would like to emphasize that limiting the time spent on the screen is important for the reduction of headache symptoms of children and adolescents.Öğe Fetal Valproate Syndrome(Elsevier Taiwan, 2017) Mutlu-Albayrak, Hatice; Bulut, Cahide; Caksen, HuseyinBackground: There have been several reports of congenital malformations in the offspring of mothers who took valproic acid (VPA) during pregnancy as a treatment for epilepsy. Methods: Herein, we describe four cases with typically similar facial features of fetal vatproate syndrome accompanied to minor skeletal abnormalities. Results: The first case was a 16-month-old girl, presenting with facial dysmorphism, and finger abnormalities. Her mother took VPA (1500 mg/d) up to the 10th gestational week and at a dosage of 1000 mg/d through the pregnancy. The second patient was 5-year-old boy with speech disability, bilateral cryptorchidism, facial dysmorphism, and finger abnormalities whose mother took VPA (1000 mg/d) through pregnancy. The third 19-month-old patient was the brother of the second patient who had facial dysmorphism, bilateral cryptorchidism, and finger abnormalities. His mother also took VPA (1000 mg/d) through pregnancy. The fourth 3-year and 6 month-old boy with minor facial dysmorphism and sternum deformity was exposed to VPA (500 mg/d) in utero. Conclusion: In conclusion, there is a recognizable spectrum of abnormalities in some infants exposed to VPA without dose-depence and the common facial dysmorphic features and minor skeletal abnormalities that may occur within the both low and high dose VPA use. Copyright (C) 2016, Taiwan Pediatric Association. Published by Elsevier Taiwan LLC.Öğe A Guide for Youth. From the Risale-i Nur Collection, (in Turkish)(Routledge Journals, Taylor & Francis Ltd, 2022) Caksen, Huseyin[Abstract Not Availabe]Öğe Importance of Religious Coping in Bereaved Parents after the Death of a Child with Genetic Disorder(Georg Thieme Verlag Kg, 2023) Caksen, Huseyin[Abstract Not Availabe]
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