Results 31 to 40 of about 2,306,494 (185)
The biopsychosocial impact of hypermobility spectrum disorders in adults: a scoping review
AbstractJoint hypermobility affects approximately 30% of the United Kingdom (UK) population, characterised by the ability to move joints beyond the physiological limits. Associated conditions include Ehlers-Danlos syndrome and hypermobility spectrum disorders, affecting individuals across physical, psychological and social levels detrimentally ...
Natalie L. Clark +4 more
openaire +4 more sources
Neurodevelopmental atypisms in the context of joint hypermobility, hypermobility spectrum disorders, and
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
This project will involve surveying adults from the United States who are diagnosed with hypermobile Ehlers-Danlos Syndrome (hEDS) or hypermobility spectrum disorder (HSD) or individuals who suspect they have one of these conditions. Participants will be
Pat Frazier +3 more
core +1 more source
A review of respiratory manifestations and their management in Ehlers-Danlos syndromes and hypermobility spectrum disorders [PDF]
Background: Ehlers-Danlos Syndromes (EDS) and Hypermobility Spectrum Disorders (HSD) are a heterogeneous group of heritable genetic connective tissue disorders with multiple characteristics including joint hypermobility, tissue fragility, and multiple organ dysfunction.
Karan Chohan +12 more
openaire +2 more sources
Neurovisceral phenotypes in the expression of psychiatric symptoms [PDF]
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
Purpose: This cross-sectional mixed-method study examined healthcare experiences among individuals in the US with hypermobile Ehlers-Danlos syndrome (hEDS) and hypermobility spectrum disorder (HSD), genetic connective tissue disorders.
Frazier, Patricia +3 more
core +1 more source
Throat and voice problems in
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
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
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
The significance of hypermobility syndromes for rheumatology [PDF]
Joint hypermobility (JHM) arises from multifactorial influences including age, gender, trauma, conditioning, infection, inflammation, and genetic factors. It frequently co-occurs with skin overstretching seen in connective tissue disorders such as Ehlers-
Jürgen Braun
doaj +1 more source

