Malformasyonu Olan Çocuk ve Ergenlerde Konsültasyon-Liyezon Psikiyatrisi

Kamra J, Jain N. Incidence of congenital malformations and its association with maternal risk factors: A prospective study. International Journal of Gynecology and Obstetrics Research. 2020;2(1): 16-20.

Ersoy F, Ersoy M, Yalçın M. Konjenital Malformasyonlara Bir Bakış. Türkiye Aile Hekimliği Dergisi. 2007;3(1-2):40-46.

Feldkamp ML, Carey JC, Byrne JL, et al. Etiology and clinical presentation of birth defects: population based study. British Medical Journal. 2017;357:j2249. doi: 10.1136/bmj.j2249.

Toufaily MH, Westgate MN, Lin AE, et al. Causes of congenital malformations. Birth defects research, 2018;110(2):87-91. doi: 10.1002/bdr2.1105.

Keeling JW, Boyd PA. Congenital abnormalities and the examination of the fetus following prenatal suspicion of congenital abnormality. In: Keeling JW (ed.) Fetal and Neonatal Pathology. London: Springer; 2001. p. 111-152.

Lazarus RS, Folkman S. Stress, appraisal and coping. New York: Springer Publishing Company, 1984.

Feng X, Lacher M, Quitmann J, et al. Health-related quality of life and psychosocial morbidity in anorectal malformation and Hirschsprung's disease. European Journal of Pediatric Surgery. 2020;30(3):279-286. doi: 10.1055/s-0040-1713597

Diseth TH, Egeland T, Emblem R. Effects of anal invasive treatment and incontinence on mental health and psychosocial functioning of adolescents with Hirschsprung's disease and low anorectal anomalies. Journal of pediatric surgery. 1998;33(3):468-475. doi: 10.1016/s0022-3468(98)90090-2.

Funakosi S, Hayashi J, Kamiyama T, et al. Psychosocial liaison-consultation for the children who have undergone repair of imperforate anus and Hirschsprung disease. Journal of pediatric surgery. 2005;40(7): 1156-1162. doi: 10.1016/j.jpedsurg.2005.03.05

Hartman EE, Oort FJ, Aronson DC. Quality of life and disease-specific functioning of patients with anorectal malformations or Hirschsprung's disease: a review. Archives of disease in childhood. 2011;96(4): 398-406. doi: 10.1136/adc.2007.118133

Senel E, Akbiyik F, Atayurt H, et al. Urological problems or fecal continence during long-term follow-up of patients with anorectal malformation. Pediatric surgery international. 2010;26(7):683-689. doi: 10.1007/s00383-010-2626-1

Akin Sari B, Demiroğullari B, Ozen O, et al. Quality of life and anxiety in Turkish patients with anorectal malformation. Journal of Paediatrics and Child Health. 2014; 50(2):107-111. doi: 10.1111/jpc.12406.

Kyrklund K, Neuvonen, MI, Pakarinen MP, et al. Social morbidity in relation to bowel functional outcomes and quality of life in anorectal malformations and Hirschsprung's disease. European Journal of Pediatric Surgery. 2018;28(06):522-528. doi: 10.1055/s-0037-1607356.

Grano C, Fernandes M, Bucci S, et al. Self‐efficacy beliefs, faecal incontinence and health‐related quality of life in patients born with anorectal malformations. Colorectal Disease, 2018;20(8):711-718. doi: 10.1111/codi.14259

Grano C, Bucci S, Aminoff D, et al. Transition from childhood to adolescence: quality of life changes 6 years later in patients born with anorectal malformations. Pediatric surgery international. 2015;31(8):735-740. doi: 10.1007/s00383-015-3736-6

Judd-Glossy L, Ariefdjohan M, Curry S, et al. A survey of adults with anorectal malformations: perspectives on educational, vocational, and psychosocial experiences. Pediatric surgery international. 2019;35(9):953-961. doi: 10.1007/s00383-019-04508-y

Stern DN. Maternal representations: A clinical and subjective phenomenological view. Infant Mental Health Journal. 1991;12(3):174-186. https://doi.org/10.1002/1097-0355(199123)12:3<174::AID-IMHJ2280120305>3.0.CO;2-0

Witvliet M, Sleeboom C, De Jong J, et al. Anxiety and quality of life of parents with children diagnosed with an anorectal malformation or Hirschsprung disease. European Journal of Pediatric Surgery. 2014;24(1):70-74. doi: 10.1055/s-0033-1353491.

Grano C, Aminoff D, Lucidi F, et al. Long-term disease-specific quality of life in adult anorectal malformation patients. Journal of pediatric surgery. 2011;46(4):691-698. doi: 10.1016/j.jpedsurg.2010.10.016

Tillman KK. Craniofacial malformations and psychiatric disorders from a neurodevelopmental perspective (Doctoral dissertation, Acta Universitatis Upsaliensis). 2020

Poling MI, Dufresne CR. Epidemiology, prevention, diagnosis, treatment, and outcomes for psychosocial problems in patients and families affected by non-intellectually impairing craniofacial malformation conditions: a systematic review protocol of qualitative data. Systematic reviews. 2019;8(1):127. doi: 10.1186/s13643-019-1045-1

Wallace ER, Collett BR, Heike CL, et al. Behavioral-social adjustment of adolescents with craniofacial microsomia. The Cleft Palate-Craniofacial Journal. 2018;55(5):664-675. doi: 10.1177/1055665617750488

Feragen KB, Stock NM. Psychological adjustment to craniofacial conditions (excluding oral clefts): a review of the literature. Psychology & health. 2017;32(3):253-288. doi: 10.1080/08870446.2016.1247838

Zerpe AS, Nowinski D, Ramklint M, et al. Parents’ Experiences of Their Child's Craniosynostosis and the Initial Care Process. Journal of Craniofacial Surgery. 2020;31(1): 251-256. doi: 10.1097/SCS.0000000000006033

Case RJ, Anderson A, Walsh R. Craniofacial anomalies and mothers’ psychological functioning: The mediating role of social support. Journal of paediatrics and child health. 2018;54(2):148-152. doi: 10.1111/jpc.13710.

Franzblau LE, Chung KC, Carlozzi N, et al. Coping with congenital hand differences. Plastic and reconstructive surgery. 2015;135(4):1067-1075. doi: 10.1097/PRS.0000000000001047.

Maddern LH, Cadogan JC, Emerson MP. ‘Outlook’: A psychological service for children with a different appearance. Clinical child psychology and psychiatry. 2006;11(3):431-443. doi: 10.1177/1359104506064987

Newell R, Marks I. Phobic nature of social difficulty in facially disfigured people. The British Journal of Psychiatry. 2000;176(2):177-181. doi: 10.1192/bjp.176.2.177

Spence SH, Donovan C, Brechman‐Toussaint M. The treatment of childhood social phobia: The effectiveness of a social skills training‐based, cognitive‐behavioural intervention, with and without parental involvement. Journal of Child Psychology and Psychiatry. 2000;41(6):713-726.

Dush DM, Hirt ML, Schroeder HE. Self-statement modification in the treatment of child behavior disorders: A meta-analysis. Psychological bulletin. 1989;106(1):97-106. doi: 10.1037/0033-2909.106.1.97

Snell C, DeMaso DR. Adaptation and Coping in Chronic Childhood Physical Illness. In: Shaw RJ, DeMaso DR (eds.) Textbook of Pediatric Psychosomatic Medicine. Washington (DC), London: American Psychiatric Publishing, Inc.; 2010. p. 21-32.

Allen R, Wasserman GA, Seidman S. Children with congenital anomalies: The preschool period. Journal of pediatric psychology. 1990;15(3):327-345. doi: 10.1093/jpepsy/15.3.327

Broder HL, Richman LC, Matheson PB. Learning disability, school achievement, and grade retention among children with cleft: a two-center study. The Cleft palate-craniofacial journal. 1998;35(2):127-131. doi: 10.1597/1545-1569_1998_035_0127_ldsaag_2.3.co_2.

Carroll P, Shute R. School peer victimization of young people with craniofacial conditions: A comparative study. Psychology, health ve medicine. 2005;10(3):291-305. doi:10.1080/13548500500093753

Grano C, Fernandes M, Aminoff D, et al. The role of coping strategies on health-related quality of life in adults with anorectal malformations. Pediatric surgery international. 2016;32(8):759-765. doi: 10.1007/s00383-016-3911-4

Brown RT, Kupst MJ. Coping with Chronic Illness in Children and Their Families. In: DeMichelis C, Ferrari M (eds) Child and Adolescent Resilience Within Medical Contexts: Integrating Research and Practice. Switzerland : Springer International Publishing, 2016. p. 267-293