
Research view
Title: | Prader–Willi syndrome psychosocial profile in an Egyptian sample: a descriptive study |
Author: | Dalia H. Ali, Safia M. Effat, Hanan Afifi and Sarah El Shakankirey |
Abstract: |
Background
Maladaptive behaviors and cognitive impairment in patients with Prader–Willi
Syndrome can affect long-term functioning of patients and their family. Understanding
difficulties underlying the maladaptive behavior allow better management. Few or no
studies were conducted on the psychological aspect of this syndrome in Egypt.
Available studies world wide suggested that the main problem in this syndrome is
cognitive and behavioral; tremendous improvement in clinical picture has been
reported through early diagnosis and management.
Objective
The aim of the study was to evaluate the psychosocial behavioral deviations and the
cognitive functions in a sample of Egyptian children with Prader–Willi syndrome.
Patients and methods
From a cross-sectional descriptive study conducted in the National Research Centre,
we included 15 of the 72 patients of both sexes with age range of 5–15 years, fulfilling
the diagnostic threshold of the modified list of Prader–Willi criteria. Detailed
cytogenetic analysis was performed by conventional cytogenetic analysis of peripheral
blood lymphocytes and fluorescent in-situ hybridization. Cognitive and psychological
profile of all patients were assessed by: (a) Wechsler Intelligence Scale for Children,
(b) Child Behavior Checklist for ages 4–18, (c) Conners’ Parent Rating Scale-Revised;
long version, and (d) Childhood Autism Rating Scale.
Results
Patients had a mean age of 8 years ( ± 2.19 SD). A total of 66.7% of the patients
showed positive deletion, 100% of the patients were mentally subnormal, and 26.3%
had autistic features. High prevalence of inattention, hyperactivity, anxiety, and social,
cognitive, and behavioral problems were evident in the patients, with more frequency
and severity in nondeletion patients.
Conclusion
Cognitive and psychological challenges are a fixed part of the Prader–Willi Syndrome
patients’ profiles. Some differences were found within different genotypes of our study group.
Keywords:
cognitive, genotype, Prader–Willi syndrome, psychosocial profile
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Journal: | Middle East Current Psychiatry 2014, 21:95–105 |
Text: | |
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