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Pisa Syndromes in Patients with Intellectual Disability [PDF]

Mental Health and Learning Disabilities Research and Practice, 2010
The aim of this report is to describe Pisa syndrome in two adults with intellectual disability. This case report is significant as, to our knowledge, Pisa syndrome has not previously been reported in an individual with intellectual disability (learning ...
Hussain, Ijaz, Ulhaq, Inam, Murthy, Sutha   +2 more
core   +4 more sources

Young People with Intellectual Disability Transitioning to Adulthood: Do Behaviour Trajectories Differ in Those with and without Down Syndrome?

PLoS ONE, 2016
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, John Taffe, Jenny Bourke, Stewart L Einfeld, Bruce J Tonge, Julian Trollor, Helen Leonard   +6 more
doaj   +2 more sources

Cancer Incidence in People With Intellectual Disability and Down Syndrome in Australia: A Cohort Study [PDF]

Cancer Medicine
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, Claire M. Vajdic, Preeyaporn Srasuebkul, Sallie‐Anne Pearson, Julian N. Trollor   +4 more
doaj   +2 more sources

Metabolic syndrome and its components in people with intellectual disability: a meta‐analysis

Journal of Intellectual Disability Research, 2020
BACKGROUND: People with intellectual disability have an increased risk for cardiovascular diseases and associated premature mortality. Metabolic syndrome (MetS) and its components are highly predictive of cardiovascular diseases.
Davy Vancampfort, Felipe Barreto Schuch, Joseph Firth   +2 more
exaly   +2 more sources

16p11.2 Duplication Syndrome - a Case Report [PDF]

Folia Medica, 2021
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, Milena Stoyanova, Rada Staneva, Mari Hachmeriyan, Lyudmila Angelova   +4 more
doaj   +3 more sources

Capgras syndrome and intellectual disability in Down Syndrome: A case report (eng)

Klinik Psikiyatri Dergisi, 2021
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

Annals of Indian Academy of Neurology, 2021
Chromosomal microdeletion syndromes usually present with neurological abnormalities, developmental delays, and various systemic abnormalities.
Seba Biswal, Preetinanda Parida, Aranya Dubbudu, Indar Kumar Sharawat, Prateek Kumar Panda   +4 more
doaj   +1 more source

Dermatoglyphics findings in intellectual disability children with down syndrome, autism spectrum disorder and attention-deficit hyperactivity disorder: A descriptive cross-sectional study

Advances in Human Biology, 2021
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, Ziske Maristka, Lusia Hayati, Rara Inggarsih, Septi Purnamasari   +4 more
doaj   +1 more source

Case Report: Non-ossifying fibromas with pathologic fractures in a patient with NONO-associated X-linked syndromic intellectual developmental disorder

Frontiers in Genetics, 2023
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, Karin Writzl, Blaž Mavčič, Blaž Mavčič, Aleš Maver, Aleš Maver, Alenka Hodžić, Borut Peterlin   +7 more
doaj   +1 more source

A new variant of MYCN gene as a cause of Feingold syndrome

Clinical Case Reports, 2022
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, Ramush Bejiqi, Abdurrahim Gerguri, Leonore Zogaj, Haki Jashari   +4 more
doaj   +1 more source