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1.
Soc Sci Med ; 277: 113889, 2021 05.
Article in English | MEDLINE | ID: mdl-33838449

ABSTRACT

OBJECTIVE: This study investigates how Syrian refugees explain and prefer to seek help for symptoms of post-traumatic stress disorder (PTSD) and depression. METHODS: We conducted five semi-structured focus group interviews based on a vignette-technique with Syrian refugees (n = 21 men, n = 10 women). The vignettes describe a fictional person suffering from symptoms of PTSD or depression in line with DSM-5 and ICD-10 criteria. RESULTS: Despite never mentioning PTSD, participants in the PTSD-interviews recognized the symptoms. They perceived them as a common reaction to extreme situations, mainly the war, the flight, and post-migratory stressors. Depression was labeled as either depression or feelings caused by social problems, and the participants were more hesitant to identify with these symptoms. Despite some differences, both the PTSD and depression vignettes were explained in terms of situational explanatory models and externally caused stress. The main finding is how participants described changing stressors resulting from migration and resettlement leading to a difference in how they would seek help in Syria and in Norway. Specifically, we found that preferred help-seeking and coping strategies are contextual. CONCLUSIONS: These findings point to the need to consider transformations following forced migration when studying aspects of explanatory models, preferred help-seeking, and coping strategies in refugee groups.


Subject(s)
Refugees , Stress Disorders, Post-Traumatic , Depression/diagnosis , Female , Humans , Male , Norway , Syria
3.
Stress Health ; 34(4): 534-544, 2018 Oct.
Article in English | MEDLINE | ID: mdl-29745024

ABSTRACT

Personnel operating in extreme environmental conditions are exposed to a variety of stressors. Whether a person adjusts to the conditions and is able to cope has implications for their psychological health. In previous extreme-environment work, temporal changes in stress, coping, and emotion have been reported. Building on previous studies, we used a diary methodology to explore temporal changes in and associations between daily events, coping strategies, and affect during a unique hyperarid desert expedition. Four participants undertaking a crossing of the Empty Quarter desert were recruited to the study. Participants completed pre-expedition, postexpedition, and 4-month follow-up questionnaires. A daily self-report diary was used to collect situational data. Time-based changes were analysed before testing predictive models linking events and coping strategies with affective responses. Findings suggest that participants had an overall positive experience. There were changes in both the events experienced and coping strategies used during the expedition. Variation in events and coping strategies significantly predicted fluctuations in positive and negative affect. Results offer valuable mechanistic information that could inform monitoring systems aimed at tracking psychological variables during operations in extreme environments. Results are discussed in relation to the novel context, diary methodology, and implications for those operating in extremes.


Subject(s)
Adaptation, Psychological/physiology , Desert Climate , Emotions/physiology , Expeditions , Adult , Desert Climate/adverse effects , Expeditions/psychology , Follow-Up Studies , Humans , Male , Middle Aged , Oman , Qatar
4.
Springerplus ; 5(1): 720, 2016.
Article in English | MEDLINE | ID: mdl-27375989

ABSTRACT

What are the factors that predict international students' destination-loyalty intention? This is the main question this paper addresses, using an online survey among 396 (short-term, N = 182) and (long-term, N = 214) international students at a Norwegian university. Structural equation model-AMOS was conducted to examine relationships among personal values, subjective well-being and destination-loyalty intentions. The results showed that: (1) universalism was positively related to subjective well-being for short-term students; and (2) subjective well-being was positively related to destination-loyalty intention for all groups. We found that relatively stable and happy individuals might be important for ensuring destination-loyalty intentions. Results also indicated that personal values that emphasize justice and equity are also important for short-term international students' well-being.

5.
Genet Couns ; 25(2): 183-7, 2014.
Article in English | MEDLINE | ID: mdl-25059017

ABSTRACT

Turner syndrome (TS) is one of the most common human chromosome abnormalities, occurring in approximately 1:2500 live female births. Short stature, ovarian dysgenesis and infertility are clinical hallmarks in the majority of patients with TS. The incidence of spontaneous puberty in TS is reported to be about one third. Precocious puberty in TS patients is very rare. Herein, we report precocious puberty in a case with TS.


Subject(s)
Chromosome Disorders , Puberty, Precocious/etiology , Turner Syndrome/complications , Child , Female , Humans , Mosaicism , Puberty, Precocious/genetics , Turner Syndrome/genetics
6.
Genet Couns ; 25(2): 231-5, 2014.
Article in English | MEDLINE | ID: mdl-25059024

ABSTRACT

The VATER/VACTERL association is typically defined by the presence of at least three of the following congenital malformations: vertebral anomalies, anal atresia, cardiac malformations, tracheo-esophageal fistula, renal anomalies, and limb abnormalities (13). We report a rare case of a monochorionic twin gestation in which one of the infants had VACTERL association. Antenatal ultrasound showed bilateral renal dysplasia and cardiac anomaly (ASD) in twin A. Twin A was noted to have the following anomalies: a single umbilical artery, limb anomaly (right hand preaxial polydactyly), vertebral anomalies (T9 and T11 butterfly vertebras, bilateral renal agenesis, bladder agenesis, anal and urethral atresia. A normal-sized stomach and normal amount of amniotic fluid were observed during the prenatal period with no other anomalies. Twin B (male) was healthy and no cardiac, renal, or congenital anomalies were demonstrated on ultrasound and physical examination. Infant A was also diagnosed as having VACTERL association because he had five of the core anomalies (V, A, C, R, L) of VACTERL association. Butterfly vertebra is an uncommon congenital spinal anomaly. To the best of our knowledge, our patient is the second case VACTERL association with butterfly vertebra in the literature.


Subject(s)
Anal Canal/abnormalities , Esophagus/abnormalities , Heart Defects, Congenital/pathology , Kidney/abnormalities , Limb Deformities, Congenital/pathology , Spine/abnormalities , Trachea/abnormalities , Twins, Monozygotic , Anal Canal/pathology , Anal Canal/surgery , Esophagus/pathology , Esophagus/surgery , Fatal Outcome , Heart Defects, Congenital/surgery , Humans , Infant, Newborn , Kidney/pathology , Kidney/surgery , Limb Deformities, Congenital/surgery , Male , Spine/pathology , Spine/surgery , Trachea/pathology , Trachea/surgery , Ultrasonography, Prenatal
7.
Genet Couns ; 25(1): 49-52, 2014.
Article in English | MEDLINE | ID: mdl-24783655

ABSTRACT

We report a case of a female baby born at 34 weeks of gestation. Birth weight was 1760 g (10th-25th centile), length 41cm (10th-25th centile) and head circumference 27cm (< 10th centile). Clinical examination revealed microcephaly, hypotelorism, micrognathia, a flat rudimentary nose, high palate, thick dysplastic low-set ears, a short neck, preaxial polydactyly of the right hand, and overriding toes. Investigations showed bilateral congenital glaucoma, alobar holoprosencephaly, severe ventriculomegaly and absence midline structures of the brain, a large atrial septal defect. The karyotype was 46,XX. The case was also diagnosed as having holoprosencephaly-polydactyly syndrome (pseudotrisomy 13) because she had alobar holoprosencephaly, preaxial polydactyly, facial dysmorfism (hypotelorism, micrognathia, a flat rudimentary nose, high palate, thick dysplastic low-set ears) and normal karyotype.


Subject(s)
Abnormalities, Multiple/pathology , Fetal Macrosomia/pathology , Glaucoma/congenital , Hand Deformities, Congenital/pathology , Holoprosencephaly/pathology , Polydactyly/pathology , Trisomy/pathology , Chromosomes, Human, Pair 13 , Female , Gestational Age , Humans , Infant, Newborn , Infant, Premature , Thumb/abnormalities
9.
Genet Couns ; 25(4): 357-61, 2014.
Article in English | MEDLINE | ID: mdl-25804012

ABSTRACT

Möbius syndrome is a rare congenital disease with a prevalence of between 0.0002 and 0.002% of births. Minimum diagnostic criteria for this disease include congenital unilateral or bilateral facial and abducens nerve paresis. Occasionally, the cranial nerves V and VIII are affected. If cranial VIII is affected, the person experiences hearing loss. Other findings in these patients that are not part of the diagnostic criteria include the involvement of other cranial nerves, malformations of orofacial structures, reductive limb anomalies, and defects of the chest wall. We herein report a newborn case with Möbius syndrome.


Subject(s)
Depressive Disorder, Major/therapy , Electroconvulsive Therapy/adverse effects , Mobius Syndrome/etiology , Pregnancy Complications/therapy , Adult , Female , Humans , Infant, Newborn , Male , Pregnancy , Pregnancy Trimester, Second
10.
Genet Couns ; 24(3): 279-82, 2013.
Article in English | MEDLINE | ID: mdl-24341142

ABSTRACT

Bamforth syndrome is a rare inherited condition whose main features are congenital hypothyroidism due to thyroid dysplasia, cleft palate, and spiky hair, with or without choanal atresia and bifid epiglottis. This syndrome is caused by mutations in the gene encoding thyroid transcription factor 2 (TTF-2). Here we report on a newborn with facial dysmorphism, cleft palate, spiky hair, congenital hypothyroidism and that are observed with Bamforth syndrome. This is the first case with Bamforth syndrome in which porencephaly has been observed.


Subject(s)
Brain Diseases/etiology , Cleft Palate/complications , Collagen Type IV/deficiency , Hair Diseases/complications , Hemiplegia/etiology , Hypothyroidism/complications , Abnormalities, Multiple/diagnosis , Brain/pathology , Brain Diseases/diagnosis , Cleft Palate/diagnosis , Consanguinity , Hair Diseases/diagnosis , Hemiplegia/diagnosis , Humans , Hypothyroidism/diagnosis , Infant, Newborn , Magnetic Resonance Imaging/methods , Male , Physical Examination/methods , Porencephaly
11.
Eur Rev Med Pharmacol Sci ; 17(19): 2594-7, 2013 Oct.
Article in English | MEDLINE | ID: mdl-24142604

ABSTRACT

AIM: Evidence that oxidative stress plays a role in the development of bronchopulmonary dysplasia (BPD). There is a close relationship between oxidative stress and inflammation. In this study, it is aimed to investigate influences of hydrocortisone used in the treatment of BPD on anti-oxidant system in preterm infants with BPD. PATIENTS AND METHODS: The study enrolled 33 infants with severe BPD who were undergone inpatient treatment in neonatal intensive care unit (NICU) of our Hospital and received therapy with hydrocortisone. Total oxidant status (TOS) and total anti-oxidant capacity (TAC) levels of infants enrolled to the study before and one week after the hydrocortisone therapy were studies and oxidative stress index levels were calculated. Pre- and post-treatment TOS, TAC and OSI index levels were statistically compared. RESULTS: In preterm infants with BPD, who were enrolled into the study, TOS and OSI index were found high, whereas TAC values were low. Following the treatment with hydrocortisone, statistically significant decrease in TOS and OSI index and statistically significant elevation in TAC levels were found in comparison with pre-treatment levels. CONCLUSIONS: The treatment with hydrocortisone, which is used for BPD, improves anti-oxidant system and reduces oxidative stress in infants with BPD. There is need for further studies in order to clarify the physio-pathogenesis.


Subject(s)
Bronchopulmonary Dysplasia/drug therapy , Hydrocortisone/therapeutic use , Oxidative Stress , Bronchopulmonary Dysplasia/metabolism , Female , Humans , Infant, Newborn , Male
12.
Genet Couns ; 24(2): 217-22, 2013.
Article in English | MEDLINE | ID: mdl-24032293

ABSTRACT

The 4q deletion syndrome is a rare chromosome deletion syndrome with a wide range of clinical phenotypes. Herein we report cases of twins (karyotype 46, XY) carrying terminal deletion of the chromosome 4 (q31qter) segment resulting in craniofacial dysmorphism, skeletal anomalies, ocular findings and cardiac defect.


Subject(s)
Abnormalities, Multiple/genetics , Chromosome Disorders/genetics , Diseases in Twins/genetics , Chromosome Deletion , Chromosome Disorders/pathology , Chromosome Disorders/physiopathology , Chromosomes, Human, Pair 4/genetics , Gestational Age , Humans , Infant, Newborn , Male , Turkey
15.
Genet Couns ; 21(3): 293-7, 2010.
Article in English | MEDLINE | ID: mdl-20964120

ABSTRACT

A trisomy 13 case with Robertsonian translocation presenting with atypical findings: Trisomy 13 is an autosomal trisomy caused by the presence of an extra copy of chromosome 13. Anomalies associated with this syndrome are severe mental retardation, coloboma, hypotonia, skeletal anomalies, midline anomalies, facial defects, holoprosencephaly, cardiac defects, omphalocele and polydactyly. Here we report a case of trisomy 13 with Robertsonian translocation, 160 day old, presenting with atypical findings like posterior fusion defect of the vertebra, hyperplasia of the right lobe of the liver, dilatation at pelvicalyxial system, scoliosis and complex heart disease including cardiomyopathy.


Subject(s)
Abnormalities, Multiple/genetics , Cardiomyopathies/genetics , Chromosome Aberrations , Chromosomes, Human, Pair 13/genetics , Heart Defects, Congenital/genetics , Liver/abnormalities , Scoliosis/genetics , Spine/abnormalities , Translocation, Genetic/genetics , Trisomy/genetics , Diagnosis, Differential , Humans , Hyperplasia/genetics , Infant , Infant, Newborn , Liver/pathology , Male , Penis/abnormalities , Polydactyly
16.
Genet Couns ; 20(3): 243-7, 2009.
Article in English | MEDLINE | ID: mdl-19852430

ABSTRACT

Toriello-Carey syndrome in a Turkish newborn: Toriello-Carey syndrome is characterized by agenesis of the corpus callosum, telecanthus, short palpebral fissures, small nose with anteverted nares, retrognathia, abnormal ears, laryngeal and cardiac anomalies, brachydactyly, and hypotonia. We describe the findings in a Turkish newborn, presumed to be another example of the Toriello-Carey syndrome, which extends the phenotype of the syndrome.


Subject(s)
Abnormalities, Multiple/genetics , Acrocallosal Syndrome/genetics , Craniofacial Abnormalities/genetics , Intellectual Disability/genetics , Abnormalities, Multiple/diagnosis , Acrocallosal Syndrome/diagnosis , Adult , Consanguinity , Craniofacial Abnormalities/diagnosis , Echoencephalography , Humans , Infant, Newborn , Intellectual Disability/diagnosis , Karyotyping , Male , Syndrome , Turkey
18.
Occup Med (Lond) ; 52(7): 383-91, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12422025

ABSTRACT

Our objective was to evaluate the effect of 12 weeks of stress management training (SMT), physical exercise (PE) and an integrated health programme (IHP) in a worksite setting on subjective health complaints. To do this, we randomly split 860 employees into the following groups: control (n = 344), PE (n = 189), IHP (comprising physical exercise and health information) (n = 165) and SMT (n = 162). There were no significant effects on subjective health complaints, sick leave or job stress. However, strong and specific positive effects were experienced for the particular goal areas defined for each intervention. The PE group showed improved general health, physical fitness and muscle pain, while the SMT group showed improved stress management. The IHP group showed the strongest effects, affecting most goals set for treatment.


Subject(s)
Exercise Therapy/methods , Stress, Psychological/prevention & control , Adaptation, Physiological , Adult , Female , Humans , Male , Norway , Occupational Health Services/standards , Patient Education as Topic , Sick Leave , Software Design , Workplace
19.
Environ Behav ; 33(1): 134-50, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11762441

ABSTRACT

Two space simulation studies for the European Space Agency found that interpersonal tension increased in the beginning, around the middle, and toward the end of the confinement. This article reports data from a third study where this issue was further examined. Three subjects were confined in the MIR space station simulator in Moscow for 135 days. Communication analysis, peer rating, questionnaires, and interviews were used to assess crew tension. The temporal pattern found in this study corresponds to the previous findings. The beginning of the period was characterized by competition over leadership. Decreased crew cohesion and aggression toward the mission control marked the middle of the confinement. In the final weeks, open conflicts emerged, and one member was socially excluded. Joking occurred frequently in the first half of the confinement, whereas negative emotional expressions increased in the second half. These results might assist planners in anticipating behavioral problems during space missions.


Subject(s)
Astronauts/psychology , Interpersonal Relations , Social Isolation/psychology , Space Simulation/psychology , Stress, Psychological/psychology , Adult , Aerospace Medicine , Communication , Group Processes , Humans , Male , Russia , Surveys and Questionnaires
20.
Gravit Space Biol Bull ; 14(2): 47-54, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11865868

ABSTRACT

As the duration of space flights increases and crews become more heterogeneous, psychosocial factors are likely to play an increasingly important role in determining mission success. The operations of the International Space Station and planning of interplanetary missions represent important future challenges for how to select, train and monitor crews. So far, empirical evidence about psychological factors in space is based on simulations and personnel in analog environments (i.e. polar expeditions, submarines). It is apparent that attempts to transfer from these environments to space requires a thorough analysis of the human behavior specific to the fields. Recommendations for research include the effects of multi-nationality on crew interaction, development of tension within crews and between Mission Control, and prediction of critical phases in adaptation over time. Selection of interpersonally compatible crews, pre-mission team training and implementation of tools for self-monitoring of psychological parameters ensure that changes in mission requirements maximize crew performance.


Subject(s)
Adaptation, Psychological , Astronauts/psychology , Interpersonal Relations , Social Isolation , Space Flight/trends , Space Simulation , Aerospace Medicine/trends , Astronauts/education , Communication , Cultural Characteristics , Group Processes , Humans , Personality , Stress, Psychological , Weightlessness
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