Results 1 to 10 of about 2,601,816 (350)
Motor Skills in Male Children with Intellectual Disability, Down Syndrome, and Autism Spectrum Disorder: A Comparative Analysis [PDF]
Introduction: Motor skill deficits in children with intellectual disabilities can disrupt sensory information processing and motor experiences, leading to limitations in various functional domains.
Mahdi Kakavan +2 more
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BackgroundYoung people with intellectual disability exhibit substantial and persistent problem behaviours compared with their non-disabled peers. The aim of this study was to compare changes in emotional and behavioural problems for young people with ...
Kitty-Rose Foley +6 more
doaj +2 more sources
Objective There is inconsistent data on cancer risk in people with intellectual disability. Our primary objective was to compare the incidence of cancer in people with and without intellectual disability.
Julian Trofimovs +4 more
doaj +2 more sources
Case Report: A female case of X-linked intellectual disability syndrome type 34 caused by a NONO frameshift variant and literature review. [PDF]
Zhang Y, Shi X, Xiao X, Yuan S, Tang J.
europepmc +3 more sources
16p11.2 Duplication Syndrome - a Case Report [PDF]
16p11.2 duplication syndrome is a rare disorder, often associated with intellectual disability, attention deficit, hyperactivity disorder, and a predisposition to epilepsy and schizophrenia.
Mariya Levkova +4 more
doaj +3 more sources
Capgras syndrome and intellectual disability in Down Syndrome: A case report (eng)
Intellectual disability, behavioral problems and Alzheimer's disease are seen in Down syndrome which is a genetic disorder. Capgras syndrome is a misidentification syndrome.
Burcu Akın Sarı
doaj +1 more source
Chromosome 1p31.1 deletion syndrome: Limited expression
Chromosomal microdeletion syndromes usually present with neurological abnormalities, developmental delays, and various systemic abnormalities.
Seba Biswal +4 more
doaj +1 more source
Introduction: Intellectual disability is a condition, in which mental development is incomplete or hindered, causing the individuals to encounter difficulties in everyday learning.
Astri Anindya Sariza +4 more
doaj +1 more source
The NONO gene encodes a nuclear protein involved in transcriptional regulation, RNA synthesis and DNA repair. Hemizygous loss-of function, de novo or maternally inherited variants in NONO have been associated with an X-linked syndromic intellectual ...
Karin Writzl +7 more
doaj +1 more source
A new variant of MYCN gene as a cause of Feingold syndrome
Feingold syndrome 1 (FS1) is a rare disorder that is inherited in autosomal dominant manner with full penetrance but with variable expressivity. The most common phenotypical features described are finger and toe anomalies, microcephaly, short stature ...
Naim Zeka +4 more
doaj +1 more source

