A boy with conduct disorder (CD), attention deficit hyperactivity disorder (ADHD), borderline intell...
A boy with conduct disorder (CD), attention deficit hyperactivity disorder (ADHD), borderline intellectual disability, and 47,XXY syndrome in combination with a 7q11.23 duplication, 11p15.5 deletion, and 20q13.33 deletion
About this item
Full title
Author / Creator
Kolaitis, Gerasimos , Bouwkamp, Christian G. , Papakonstantinou, Alexia , Otheiti, Ioanna , Belivanaki, Maria , Haritaki, Styliani , Korpa, Terpsihori , Albani, Zinovia , Terzioglou, Elena , Apostola, Polyxeni , Skamnaki, Aggeliki , Xaidara, Athena , Kosma, Konstantina , Kitsiou-Tzeli, Sophia and Tzetis, Maria
Publisher
England: BioMed Central Ltd
Journal title
Language
English
Formats
Publication information
Publisher
England: BioMed Central Ltd
Subjects
More information
Scope and Contents
Contents
This is a case with multiple chromosomal aberrations which are likely etiological for the observed psychiatric phenotype consisting of attention deficit hyperactivity and conduct disorders.
We report on an 11 year-old boy, admitted to the pediatric hospital for behavioral difficulties and a delayed neurodevelopmental trajectory. A cytogenetic an...
Alternative Titles
Full title
A boy with conduct disorder (CD), attention deficit hyperactivity disorder (ADHD), borderline intellectual disability, and 47,XXY syndrome in combination with a 7q11.23 duplication, 11p15.5 deletion, and 20q13.33 deletion
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5024517
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5024517
Other Identifiers
ISSN
1753-2000
E-ISSN
1753-2000
DOI
10.1186/s13034-016-0121-8
