Social adjustment of children with a severe craniofacial anomaly (Apert syndrome)

被引:20
|
作者
Sarimski, K [1 ]
机构
[1] Kinderzentrum Munchen, D-81377 Munich, Germany
关键词
craniofacial anomaly; social problems; attentional problems;
D O I
10.1046/j.1365-2214.2001.00224.x
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Objective Children with a severe craniofacial anomaly are at risk for emotional and behavioural problems. Do children with Apert syndrome present with a special psychological profile? Method Parent reports (Child Behaviour Checklist) were obtained from 25 children with Apert syndrome. Results Fourteen children were characterized by clinically significant social problems, 10 by attentional problems, nine by social withdrawal. Total CBCL-scores were in the clinical range for eight children. Conclusion Information on psychosocial state should be included in regular check-ups of children with a severe craniofacial anomaly in order to identify children who are in need of psychological interventions.
引用
收藏
页码:583 / 590
页数:8
相关论文
共 50 条
  • [31] Cognitive functioning of young children with Apert's syndrome
    Sarimski, K
    GENETIC COUNSELING, 1997, 8 (04): : 317 - 322
  • [32] Dental approach for Apert syndrome in children: A systematic review
    Lopez-Estudillo, Andrea-Stacy
    Rosales-Berber, Miguel-Angel
    Ruiz-Rodriguez, Socorro
    Pozos-Guillen, Amaury
    Noyola-Frias, Miguel-Angel
    Garrocho-Rangel, Arturo
    MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL, 2017, 22 (06): : E660 - E668
  • [33] Children with Apert syndrome: behavioural problems and family stress
    Sarimski, K
    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 1998, 40 (01): : 44 - 49
  • [34] Behavioral Adjustment of Preschool Children With and Without Craniofacial Microsomia
    Johns, Alexis L.
    Wallace, Erin R.
    Collett, Brent R.
    Kapp-Simon, Kathleen A.
    Drake, Amelia F.
    Heike, Carrie L.
    Kinter, Sara L.
    Luquetti, Daniela, V
    Magee, Leanne
    Norton, Susan
    Sie, Kathleen
    Speltz, Matthew L.
    CLEFT PALATE CRANIOFACIAL JOURNAL, 2021, 58 (01): : 42 - 53
  • [35] Craniofacial Stability in Patients With Crouzon or Apert Syndrome After Le Fort III Distraction Osteogenesis
    Reitsma, Jacobus H.
    Ongkosuwito, Edwin M.
    Buschang, Peter H.
    Adrichem, Leon N. A. v
    Prahl-Andersen, Birte
    CLEFT PALATE-CRANIOFACIAL JOURNAL, 2013, 50 (05): : 561 - 569
  • [36] Apert Syndrome: Outcomes From the Australian Craniofacial Unit's Birth to Maturity Management Protocol
    David, David J.
    Anderson, Peter
    Flapper, Walter
    Syme-Grant, Jonathan
    Santoreneos, Steven
    Moore, Mark
    JOURNAL OF CRANIOFACIAL SURGERY, 2016, 27 (05) : 1125 - 1134
  • [37] A SEVERE CRANIOFACIAL IMPALEMENT INJURY (JAELS SYNDROME)
    MCKECHNIE, J
    BRITISH JOURNAL OF ORAL & MAXILLOFACIAL SURGERY, 1986, 24 (04): : 258 - 264
  • [38] THE ASSOCIATION OF IMMUNODEFICIENCY IN CHILDREN WITH SEVERE CRANIOFACIAL ANOMALIES
    MILLER, GC
    SAY, B
    AMERICAN JOURNAL OF HUMAN GENETICS, 1980, 32 (06) : A158 - A158
  • [39] CRANIOFACIAL MORPHOLOGY OF CHILDREN WITH WILLIAMS SYNDROME
    MASS, E
    BELOSTOKY, L
    CLEFT PALATE-CRANIOFACIAL JOURNAL, 1993, 30 (03): : 343 - 349
  • [40] Perioperative complications in children with Apert syndrome: a review of 509 anesthetics
    Barnett, Sarah
    Moloney, Claire
    Bingham, Robert
    PEDIATRIC ANESTHESIA, 2011, 21 (01) : 72 - 77