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Emotional functioning among children with neurofibromatosis type 1 or Noonan syndrome.
McNeill, Alana M; Hudock, Rebekah L; Foy, Allison M H; Shanley, Ryan; Semrud-Clikeman, Margaret; Pierpont, Mary Ella; Berry, Susan A; Sommer, Katherine; Moertel, Christopher L; Pierpont, Elizabeth I.
Afiliação
  • McNeill AM; Division of Clinical Behavioral Neuroscience, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota.
  • Hudock RL; Division of Clinical Behavioral Neuroscience, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota.
  • Foy AMH; Division of Clinical Behavioral Neuroscience, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota.
  • Shanley R; Department of Educational Psychology, University of Wisconsin-Madison, Madison, Wisconsin.
  • Semrud-Clikeman M; Biostatistics Core, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
  • Pierpont ME; Division of Clinical Behavioral Neuroscience, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota.
  • Berry SA; Division of Genetics and Metabolism, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota.
  • Sommer K; Division of Genetics and Metabolism, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota.
  • Moertel CL; Division of Hematology and Oncology, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota.
  • Pierpont EI; Division of Hematology and Oncology, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota.
Am J Med Genet A ; 179(12): 2433-2446, 2019 12.
Article em En | MEDLINE | ID: mdl-31566897
While neurofibromatosis type 1 (NF1) and Noonan syndrome (NS) are clinically distinct genetic syndromes, they have overlapping features because they are caused by pathogenic variants in genes encoding molecules within the Ras-mitogen-activated protein kinase signaling pathway. Increased risk for emotional and behavioral challenges has been reported in both children and adults with these syndromes. The current study examined parent-report and self-report measures of emotional functioning among children with NF1 and NS as compared to their unaffected siblings. Parents and children with NS (n = 39), NF1 (n = 39), and their siblings without a genetic condition (n = 32) completed well-validated clinical symptom rating scales. Results from parent questionnaires indicated greater symptomatology on scales measuring internalizing behaviors and symptoms of attention deficit hyperactivity disorder (ADHD) in both syndrome groups as compared with unaffected children. Frequency and severity of emotional and behavioral symptoms were remarkably similar across the two clinical groups. Symptoms of depression and anxiety were higher in children who were also rated as meeting symptom criteria for ADHD. While self-report ratings by children generally correlated with parent ratings, symptom severity was less pronounced. Among unaffected siblings, parent ratings indicated higher than expected levels of anxiety. Study findings may assist with guiding family-based interventions to address emotional challenges.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neurofibromatose 1 / Emoções / Síndrome de Noonan Tipo de estudo: Prognostic_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neurofibromatose 1 / Emoções / Síndrome de Noonan Tipo de estudo: Prognostic_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Ano de publicação: 2019 Tipo de documento: Article