Results 31 to 40 of about 1,777,874 (197)

Neurodevelopmental atypisms in the context of joint hypermobility, hypermobility spectrum disorders, andEhlers–Danlossyndromes [PDF]

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2021
AbstractJoint hypermobility (JHM), defined as an increased range of joint motion, is a frequent somatic trait in the general population but also the hallmark of many of the hereditary disorders of connective tissue. Ehlers–Danlos syndromes (EDS) belong to this group of diseases and are characterized by tissue fragility, skin abnormalities, and JHM ...
openaire   +2 more sources

Neurovisceral phenotypes in the expression of psychiatric symptoms [PDF]

open access: yes, 2015
This review explores the proposal that vulnerability to psychological symptoms, particularly anxiety, originates in constitutional differences in the control of bodily state, exemplified by a set of conditions that include Joint Hypermobility, Postural ...
Satoshi Umeda (291576)   +19 more
core   +1 more source

Adaptation of balance reactions following forward perturbations in people with joint hypermobility syndrome

open access: yesBMC Musculoskeletal Disorders, 2021
Background Joint Hypermobility Syndrome (JHS) is a Heritable Disorder of Connective tissue characterised by joint laxity and chronic widespread arthralgia. People with JHS exhibit a range of other symptoms including balance problems.
Alexander Vernon Bates   +2 more
doaj   +1 more source

Folate-dependent hypermobility syndrome: A proposed mechanism and diagnosis

open access: yesHeliyon, 2023
Hypermobility involves excessive flexibility and systemic manifestations of connective tissue fragility. We propose a folate-dependent hypermobility syndrome model based on clinical observations, and through a review of existing literature, we raise the ...
Jacques Courseault   +7 more
doaj   +1 more source

Throat and voice problems inEhlers–Danlossyndromes and hypermobility spectrum disorders [PDF]

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2021
AbstractA small number of case reports and observational studies describe chronic nasal congestion, upper airway obstruction, dysphonia, vocal cord abnormalities, and swallowing abnormalities in the Ehlers–Danlos syndromes. Little is known of the causes and therefore treatments of these, yet they are not uncommon findings in persons with hypermobility ...
Martin A. Birchall   +2 more
openaire   +2 more sources

Gender ratio in a clinical population sample, age of diagnosis and duration of assessment in children and adults with autism spectrum disorder. [PDF]

open access: yes, 2016
This article reports on gender ratio, age of diagnosis and the duration of assessment procedures in autism spectrum disorder diagnosis in a national study which included all types of clinical services for children and adults. Findings are reported from a
Rutherford, Marion   +19 more
core   +1 more source

The Subjective Experience of Music in Autism Spectrum Disorder [PDF]

open access: yes, 2009
Semi-structured interviews were conducted with 12 high-functioning adults on the autism spectrum in order to examine the nature of their personal experiences of music. The analysis showed that most participants exploit music for a wide range of purposes
Rory Allen   +5 more
core   +1 more source

Migration and autism spectrum disorder: population-based study. [PDF]

open access: yes, 2012
BACKGROUND: Migration has been implicated as a risk factor for autism, but evidence is limited and inconsistent. AIMS: To investigate the relationship between parental migration status and risk of autism spectrum disorder, taking into consideration the ...
Goodman, Anna   +25 more
core   +1 more source

The Role of Cell Adhesion and Cytoskeleton Dynamics in the Pathogenesis of the Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders

open access: yesFrontiers in Cell and Developmental Biology, 2021
The Ehlers-Danlos syndromes (EDS) are a group of 13 disorders, clinically defined through features of joint hypermobility, skin hyperextensibility, and tissue fragility. Most subtypes are caused by mutations in genes affecting the structure or processing
Sabeeha Malek, Darius V. Köster
doaj   +1 more source

Updates in Clinical and Genetics Aspects of Hypermobile Ehlers Danlos Syndrome

open access: yesBalkan Medical Journal, 2019
Efforts on recognition, diagnosis, and management of the presumed, most common connective tissue disorder hypermobile Ehlers-Danlos syndrome have been an ongoing challenge, even decades after the description of this condition.
Irman Forghani
doaj   +1 more source

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