Down Syndrome Neuropsychological Phenotype across the Lifespan
Down syndrome (DS), caused by the triplication of chromosome 21, is the most common genetic cause of intellectual disability (ID). Individuals with DS commonly exhibit unique neuropsychological profiles that emerge during specific developmental stages across the lifespan, often characterized by earl...
Saved in:
Other Authors: | |
---|---|
Format: | Electronic Book Chapter |
Language: | English |
Published: |
Basel
MDPI - Multidisciplinary Digital Publishing Institute
2022
|
Subjects: | |
Online Access: | DOAB: download the publication DOAB: description of the publication |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
MARC
LEADER | 00000naaaa2200000uu 4500 | ||
---|---|---|---|
001 | doab_20_500_12854_84448 | ||
005 | 20220621 | ||
003 | oapen | ||
006 | m o d | ||
007 | cr|mn|---annan | ||
008 | 20220621s2022 xx |||||o ||| 0|eng d | ||
020 | |a books978-3-0365-3961-4 | ||
020 | |a 9783036539621 | ||
020 | |a 9783036539614 | ||
040 | |a oapen |c oapen | ||
024 | 7 | |a 10.3390/books978-3-0365-3961-4 |c doi | |
041 | 0 | |a eng | |
042 | |a dc | ||
072 | 7 | |a M |2 bicssc | |
072 | 7 | |a PSAN |2 bicssc | |
100 | 1 | |a Pulsifer, Margaret B. |4 edt | |
700 | 1 | |a Pulsifer, Margaret B. |4 oth | |
245 | 1 | 0 | |a Down Syndrome |b Neuropsychological Phenotype across the Lifespan |
260 | |a Basel |b MDPI - Multidisciplinary Digital Publishing Institute |c 2022 | ||
300 | |a 1 electronic resource (180 p.) | ||
336 | |a text |b txt |2 rdacontent | ||
337 | |a computer |b c |2 rdamedia | ||
338 | |a online resource |b cr |2 rdacarrier | ||
506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
520 | |a Down syndrome (DS), caused by the triplication of chromosome 21, is the most common genetic cause of intellectual disability (ID). Individuals with DS commonly exhibit unique neuropsychological profiles that emerge during specific developmental stages across the lifespan, often characterized by early developmental delay, cognitive strengths and weaknesses, behavior and mental health issues, and age-related cognitive decline, frequently resulting in early-onset Alzheimer's disease. These profiles are unique compared to other individuals with ID and reflect the genetic mechanisms and neuroanatomic features underlying the distinct neuropsychological phenotype associated with DS. This Special Issue aims to highlight the recent advancements in understanding the neuropsychological phenotype associated with DS across the lifespan. The lifespan perspective will cover four developmental stages: (1) early childhood; (2) school age; (3) young adulthood, and (4) older adulthood. Authors contributed cutting-edge original research studies and comprehensive reviews that address a broad range of topics related to DS, including early developmental trajectories, cognitive functioning, language, adaptive skills, behavior and mental health, assessment and diagnosis, age-related cognitive decline, and medical issues related to the neuropsychological phenotype and neuroimaging. | ||
540 | |a Creative Commons |f https://creativecommons.org/licenses/by/4.0/ |2 cc |4 https://creativecommons.org/licenses/by/4.0/ | ||
546 | |a English | ||
650 | 7 | |a Medicine |2 bicssc | |
650 | 7 | |a Neurosciences |2 bicssc | |
653 | |a trisomy 21 | ||
653 | |a decoding | ||
653 | |a vocabulary | ||
653 | |a letters | ||
653 | |a phonological awareness | ||
653 | |a down syndrome | ||
653 | |a fluency | ||
653 | |a disfluency | ||
653 | |a co-occurrence | ||
653 | |a comorbidity | ||
653 | |a language | ||
653 | |a Down syndrome | ||
653 | |a social cognition | ||
653 | |a social behavior | ||
653 | |a measurement | ||
653 | |a children | ||
653 | |a attention | ||
653 | |a audiovisual processing | ||
653 | |a communicative abilities in infants | ||
653 | |a Trisomy 21 | ||
653 | |a independence | ||
653 | |a transition to adulthood | ||
653 | |a proxy-report | ||
653 | |a regression | ||
653 | |a Alzheimer's disease | ||
653 | |a biomarkers | ||
653 | |a dementia | ||
653 | |a cognition | ||
653 | |a functional independence | ||
653 | |a neuropsychological assessment | ||
653 | |a primary care | ||
653 | |a screening | ||
653 | |a early regression | ||
653 | |a idiopathic regression | ||
653 | |a depression | ||
653 | |a selective serotonin reuptake inhibitor | ||
653 | |a mild cognitive impairment | ||
653 | |a cognitive decline | ||
653 | |a neuropsychological tests | ||
653 | |a cognitive function | ||
653 | |a early-onset Alzheimer disease | ||
653 | |a late-onset Alzheimer disease | ||
653 | |a hypothyroidism | ||
653 | |a thyroid autoantibodies | ||
653 | |a TSH | ||
653 | |a Free T4 | ||
653 | |a APOE Ɛ4 | ||
653 | |a autism spectrum disorder | ||
653 | |a co-occurring | ||
653 | |a prevalence | ||
653 | |a n/a | ||
856 | 4 | 0 | |a www.oapen.org |u https://mdpi.com/books/pdfview/book/5431 |7 0 |z DOAB: download the publication |
856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/84448 |7 0 |z DOAB: description of the publication |