Results 41 to 50 of about 855,411 (199)

Temporomandibular disorder and generalized joint hypermobility: application of diagnostic criteria [PDF]

open access: yesBrazilian Journal of Otorhinolaryngology, 2011
Generalized joint hypermobility (GJH) has been considered a predisposing factor for the development of temporomandibular disorder (TMD).To evaluate clinical and psychosocial aspects in individuals diagnosed with TMD with or without GJH.Clinical and experimental study, which enrolled 34 women, from 18 to 35 years of age with TMD diagnosed by RDC/TMD ...
Pasinato, Fernanda   +3 more
openaire   +4 more sources

Editorial Commentary: Diagnosis and Treatment of Generalized Joint Hypermobility in Patients With Anterior Cruciate Ligament Injury

open access: yes, 2021
Generalized joint hypermobility (GJH), or laxity, is defined as hyperextensibility of the synovial joints. Hypermobility is caused by alterations in the connective tissues, in turn caused by various factors including impaired function of collagen ...
Sundemo, David,   +2 more
core   +1 more source

Prevalence of joint hypermobility, hypermobility spectrum disorder and hypermobile Ehlers-Danlos syndrome in a university population: an observational study

open access: yes, 2020
Objectives: To investigate the prevalence of joint hypermobility classes, hypermobility spectrum disorders,hypermobile Ehlers-Danlos syndrome and their relations with sex ina university population.
Filiz TUNA, Tuna, Filiz
core   +1 more source

A Novel Homozygous Nonsense Variant in DCHS1 in a Brazilian Patient With Van Maldergem Syndrome Type 1: Clinical Report and Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Van Maldergem syndrome (VMLDS) is an ultra‐rare autosomal recessive disorder characterized by craniofacial dysmorphism, intellectual disability, hypotonia, skeletal anomalies, and feeding difficulties. It is caused by biallelic variants in DCHS1 or FAT4 genes.
Gabriela Roldão Correia‐Costa   +4 more
wiley   +1 more source

The EXPLAIN Study: Exploring Arthrogryposis Multiplex Congenita in Adults in Norway — A Description of Demographic, Medical, and Neurological Findings

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis Multiplex Congenita (AMC) encompasses several hundred conditions with diverse genetic, pathophysiological, and clinical origins. The overarching EXPLAIN study explores underlying causes and implications of AMC and represents the largest clinical cohort of adults with AMC reported to date.
My Vuong Hermansen   +5 more
wiley   +1 more source

Gait pattern in 9-11-year-old children with generalized joint hypermobility compared with controls; a cross-sectional study [PDF]

open access: yes, 2013
To study differences in gait patterns in 10-year-old children with Generalized Joint Hypermobility (GJH) and with no GJH (NGJH)
Peter Kastmand Larsen   +18 more
core   +2 more sources

Human evolution and the obstetrical dilemma: The pelvic floor hypothesis

open access: yesThe Anatomical Record, EarlyView.
Abstract Human childbirth is mechanically difficult because a large‐headed, broad‐shouldered fetus must pass through a comparatively narrow, twisted bony birth canal. Traditional explanations of this “obstetrical dilemma” emphasize the role of bipedal locomotion in inhibiting the evolution of a wider, more spacious pelvis.
Barbara Fischer, Ekaterina Stansfield
wiley   +1 more source

Association between generalized hypermobility of joint and hypermobility temporomandibular joint (TMJ) [PDF]

open access: yes, 2011
Hypermobility TMJ is characterized by increase in a mobility, to proceed asymptoms, articulate sounds, discomfort, blocking joint at function. Increase in mobility proportionally expressivenesses generalized hypermobility of joints.Цель исследования ...
Костина, И. Н., Kostina, I. N.
core  

A severe case of PLOD1‐related kyphoscoliotic Ehlers–Danlos syndrome associated with several arterial and venous complications: A case report

open access: yesClinical Case Reports, 2023
Kyphoscoliotic Ehlers–Danlos syndrome (kEDS) is a rare genetic disorder combining congenital hypotonia, congenital/early onset and progressive kyphoscoliosis, and generalized joint hypermobility.
Malika Foy   +13 more
doaj   +1 more source

Anatomic and Histologic Analyses of the Popliteal Hiatus Area of the Lateral Meniscus Reveal the Meniscofibular Ligament and the Posteroinferior Popliteomeniscal Fascicle Are Ligamentous Tissue

open access: yesArthroscopy, EarlyView.
Purpose To characterize the anatomical structure and histological composition of connective tissue around the popliteal hiatus of the lateral meniscus (LM): the posterosuperior popliteomeniscal fascicle (PS‐PMF), posteroinferior popliteomeniscal fascicle (PI‐PMF), and anterior popliteomeniscal fascicle (A‐PMF), meniscofibular ligament (MFL), and ...
Heng Zhu   +6 more
wiley   +1 more source

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