Cognitive outcome after complicated mild traumatic brain injury: A literature review and meta-analysis

D Hacker, CA Jones, E Yasin, S Preece… - Journal of …, 2023 - liebertpub.com
Cognitive outcome for mild traumatic brain injury (mTBI) with positive brain imaging
(complicated mTBI) was compared with that for mTBI with normal imaging (uncomplicated …

A Comprehensive Review of Syndromic Forms of Obesity: Genetic Etiology, Clinical Features and Molecular Diagnosis

LML Carvalho, AAL Jorge, DR Bertola… - Current Obesity …, 2024 - Springer
Syndromic obesity refers to obesity occurring with additional clinical findings, such as
intellectual disability/developmental delay, dysmorphic features, and congenital …

'Playing a guessing game': Recognising and responding to anxiety in children with intellectual disability

G Fynn, M Porter, E Pellicano - Journal of Applied Research in …, 2023 - Wiley Online Library
Background Children with intellectual disability are at greater risk of developing anxiety than
the general population. Limited research has examined the challenges associated with …

[HTML][HTML] Neurobehavioral phenotype of Kabuki syndrome: Anxiety is a common feature

AJ Kalinousky, T Rapp, H Hijazi, J Johnson… - Frontiers in …, 2022 - frontiersin.org
Kabuki syndrome (KS) is a Mendelian Disorder of the Epigenetic Machinery (MDEM) caused
by loss of function variants in either of two genes involved in the regulation of histone …

[HTML][HTML] Combined extended reality and reinforcement learning to promote healthcare and reduce social anxiety in fragile X syndrome: a new assessment tool and a …

F Stasolla, A Passaro, M Di Gioia, E Curcio… - Frontiers in …, 2023 - frontiersin.org
Fragile X syndrome (FXS) is a rare genetic disease caused by mutations in the fifth
untranslated region of the FMRI gene situated on the Xq27. 3 site, resulting in an expansion …

[HTML][HTML] Identification of molecular signatures and pathways involved in Rett syndrome using a multi-omics approach

A Pascual-Alonso, C Xiol, D Smirnov, R Kopajtich… - Human Genomics, 2023 - Springer
Background Rett syndrome (RTT) is a neurodevelopmental disorder mainly caused by
mutations in the methyl-CpG-binding protein 2 gene (MECP2). MeCP2 is a multi-functional …

[HTML][HTML] Behavioural and physiological indicators of anxiety reflect shared and distinct profiles across individuals with neurogenetic syndromes

H Crawford, C Oliver, L Groves, L Bradley, K Smith… - Psychiatry …, 2023 - Elsevier
Anxiety is heightened in individuals with intellectual disability, particularly in those with
specific neurogenetic syndromes. Assessment of anxiety for these individuals is hampered …

[HTML][HTML] Behaviours that challenge in SATB2-associated syndrome: correlates of self-injury, aggression and property destruction

L Shelley, J Waite, J Tarver, C Oliver… - Journal of autism and …, 2023 - Springer
Abstract SATB2-associated syndrome (SAS) is a genetic syndrome characterised by
intellectual disability, severe speech delay, and palatal and dental problems. Behaviours …

Speech and language in DDX3Xneurodevelopmental disorder: A call for early augmentative and alternative communication intervention

EJ Forbes, LD Morison, F Lelik, T Howell… - American Journal of …, 2024 - Wiley Online Library
Pathogenic variants in DDX3X are associated with neurodevelopmental disorders.
Communication impairments are commonly reported, yet specific speech and language …

Anxiety and depression During the COVID-19 Pandemic and Their Impact on Sleep

M Al Maqbali - COVID-19 and Sleep: A Global Outlook, 2023 - Springer
The effects of COVID-19 on mental health are severe. It is widely acknowledged that there is
a link between anxiety, depression, and sleep disorders. Although we are aware that such …