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1.
Am J Med Genet A ; 170(8): 1974-88, 2016 08.
Article in English | MEDLINE | ID: mdl-27149079

ABSTRACT

The present study is an investigation of behavioral functioning in children with cardiofaciocutaneous syndrome (CFC). CFC is a rare single-gene disorder associated with cardiac disease, characteristic skin and facial features, intellectual disability, and neurological complications such as seizures and structural brain anomalies. Emotional and behavioral features of CFC have not been systematically investigated. We aimed to identify key variables that contribute to psychopathology during childhood and adolescence, and to examine the impact of challenging behaviors on the caregiving experience. Parents of 34 children and adolescents with CFC completed standardized broadband measures of child emotional and behavioral functioning, as well as measures of sensory modulation, functional communication, and caregiver stress. Results indicate that children with CFC syndrome are at heightened risk for psychopathology, with attention problems, social difficulties, and unusual behaviors (e.g., obsessive thoughts, strange behaviors, repetitive acts) found to be especially prevalent. Behavioral challenges in children with CFC syndrome were significantly associated with a history of obstetric complications and with problems modulating sensory information. With regard to the impact of child neurocognitive and behavioral issues on the caregiving experience, parent self-reported stress was significantly higher among parents of children who engaged in more problem behaviors, and lower among parents whose children could communicate effectively with others. Results of this study suggest avenues to help families cope with CFC-related stressors and enhance overall functioning. In particular, this study highlights the need for educational and treatment interventions aimed at addressing sensory needs, increasing functional communication, and identifying and managing challenging behaviors. © 2016 Wiley Periodicals, Inc.


Subject(s)
Behavior , Ectodermal Dysplasia/diagnosis , Failure to Thrive/diagnosis , Heart Defects, Congenital/diagnosis , Phenotype , Adolescent , Caregivers/psychology , Checklist , Child , Child Behavior , Child Behavior Disorders/diagnosis , Child Behavior Disorders/genetics , Communication , Ectodermal Dysplasia/genetics , Facies , Failure to Thrive/genetics , Female , Genetic Association Studies , Genetic Predisposition to Disease , Heart Defects, Congenital/genetics , Humans , Male , Parenting , Risk Factors , Stress, Psychological
2.
Pediatrics ; 134(4): e1149-62, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25180280

ABSTRACT

Cardio-facio-cutaneous syndrome (CFC) is one of the RASopathies that bears many clinical features in common with the other syndromes in this group, most notably Noonan syndrome and Costello syndrome. CFC is genetically heterogeneous and caused by gene mutations in the Ras/mitogen-activated protein kinase pathway. The major features of CFC include characteristic craniofacial dysmorphology, congenital heart disease, dermatologic abnormalities, growth retardation, and intellectual disability. It is essential that this condition be differentiated from other RASopathies, as a correct diagnosis is important for appropriate medical management and determining recurrence risk. Children and adults with CFC require multidisciplinary care from specialists, and the need for comprehensive management has been apparent to families and health care professionals caring for affected individuals. To address this need, CFC International, a nonprofit family support organization that provides a forum for information, support, and facilitation of research in basic medical and social issues affecting individuals with CFC, organized a consensus conference. Experts in multiple medical specialties provided clinical management guidelines for pediatricians and other care providers. These guidelines will assist in an accurate diagnosis of individuals with CFC, provide best practice recommendations, and facilitate long-term medical care.


Subject(s)
Disease Management , Ectodermal Dysplasia/diagnosis , Ectodermal Dysplasia/therapy , Failure to Thrive/diagnosis , Failure to Thrive/therapy , Heart Defects, Congenital/diagnosis , Heart Defects, Congenital/therapy , Practice Guidelines as Topic/standards , Diagnosis, Differential , Ectodermal Dysplasia/genetics , Facies , Failure to Thrive/genetics , Genetic Testing/methods , Heart Defects, Congenital/genetics , Humans
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