Neurodevelopmental Disorder
Types. Neurodevelopmental disorders are impairments of the growth and development of the brain and/or central nervous system. A narrower use of the term refers to a disorder of brain function that affects emotion, learning ability, self-control and memory which unfolds as an individual develops and grows.
Cluster Number:
Wiki Number: PW131
Diagnosis: Neurodevelopmental Disorders
US Patients:
World Patients:
Sex Ratio:
Age Onset:
Brain Area:
Symptoms: a general title for fetal difficulties and damages to the brain and central nervous system:limits emotion, learning, control, etc.
Progression: many disorders, spectra and syndromes. Genetic testing after birth is needed to confirm their occurrences.
Causes: Romanian orphanages left social and language depriviation; genetics (Down and Fragile X Syndromes; immunie reactions; infectious
Medications: diseases; metabolic or nutrition disorders; physical traumas causing brain injuries within the placentas
Therapies:
Amazon or Library Book: Neurodevelopmental Disorders
Amazon or Library Book: Assessment and Diagnosis of Neurodevelopmental Disorders in Young Children
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4 CURRENT ARTICLES
FROM PUBMED
The world-wide medical research
reports chosen for each diagnosis
Clicking each title opens the
PubMed article’s summary-abstract.
- Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (MRXSHG)by Mohammad-Reza Ghasemi on December 21, 2024
The Houge type of X-linked syndromic intellectual developmental disorder (MRXSHG) encompasses a spectrum of neurodevelopmental disorders characterized by intellectual disability (ID), language/speech delay, attention issues, and epilepsy. These conditions arise from hemizygous or heterozygous deletions, along with point mutations, affecting CNKSR2, a gene located at Xp22.12. CNKSR2, also known as CNK2 or MAGUIN, functions as a synaptic scaffolding molecule within the neuronal postsynaptic...
- The challenge and promise of disentangling neurodevelopmental conditions a commentary on Davis et al. (2024)by Joe Bathelt on December 21, 2024
This commentary evaluates the study by Davis et al. on the early behavioural manifestations of autism spectrum condition (ASC) and attention deficit hyperactivity disorder (ADHD) in preschool children. Davis et al. show how children who later receive dual diagnoses exhibit significantly more severe symptoms and greater behavioural challenges compared to their peers. The study's methodological strengths, including its prospective longitudinal design and well-validated measures, are highlighted....
- RORA-neurodevelopmental disorder: a unique triad of developmental disability, cerebellar anomalies, and myoclonic seizuresby Mariagrazia Talarico on December 21, 2024
CONCLUSION: Missense variants in DBD correlate to a more severe cerebellar phenotype. The RORA-NDD triad comprises developmental disability, cerebellar features and a spectrum of myoclonic epilepsy.
- Aberrant brain structural-functional coupling and structural/functional network topology explain developmental delays in pediatric Prader-Willi syndromeby Zhongxin Huang on December 20, 2024
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder characterized by dysplasia in early life. Psychoradiology studies have suggested that mental and behavioral deficits in individuals with PWS are linked to abnormalities in brain structural and functional networks. However, little is known about changes in network-based structural-functional coupling and structural/functional topological properties and their correlations with developmental scales in children with PWS. Here, we acquired...