Results 41 to 50 of about 2,191,147 (178)

The Language of Pain in the Hypermobile Ehlers–Danlos Syndrome: Metaphors as a Key to Understanding the Experience of Pain and as a Rehabilitation Tool

Brain Sciences, 2023
Ehlers–Danlos syndromes are a heterogeneous group of Heritable Connective Tissue Disorders characterized by joint hypermobility, skin hyperextensibility, and tissue fragility.
Filippo Camerota, Rachele Mariani, Giulia Cordiano, Michela Di Trani, Valentina Lodato, Alessandro Ferraris, Massimo Pasquini, Claudia Celletti   +7 more
doaj   +1 more source

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

, 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, Alkjær, Tine, Juul-Kristensen, Birgit; id_orcid, Birgit Juul-Kristensen, Kristensen, Jens Halkjær, Falkerslev, Simon, Helene Nikolajsen, Juul-Kristensen, Birgit, Remvig, Lars, Simonsen, Erik Bruun, Nikolajsen, Helene, Jensen, Bente Rona, Erik Bruun Simonsen, Lars Remvig, Tine Alkjær, Larsen, Peter Kastmand, Bente Rona Jensen, Simon Falkerslev, Jens Halkjær Kristensen   +18 more
core   +2 more sources

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

American 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, Bruna Fagundes Rodrigues Alaite, Vera Lúcia Gil‐da‐Silva‐Lopes, Carlos Eduardo Steiner, Társis Paiva Vieira   +4 more
wiley   +1 more source

Physical therapy of children with particular systemic lesion based on the undifferentiated connective tissue dysplasia

Слобожанський науково-спортивний вісник, 2019
Purpose: to develop and prove the effectiveness of a comprehensive physical therapy program for children with systemic visual and musculoskeletal lesions based on the undifferentiated connective tissue dysplasia.
Yuliia Rudenko, Oleksandr Zviriaka, Yuliia Arieshyna   +2 more
doaj   +1 more source

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

Clinical 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, Corinne Métay, Michael Frank, Nicolas Denarié, Salma Adham, Clarisse Billon, Anne Legrand, Xavier Jeunemaitre, Fabrice Gillas, Karen Gaudon, Philippe De Mazancourt, Ahmed Mekki, Robert Carlier, Karelle Benistan   +13 more
doaj   +1 more source

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

American 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, Kristin Ørstavik, Unni Steen, Mathias Toft, Cathrine Brunborg, Lena Lande Wekre   +5 more
wiley   +1 more source

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

, 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,, Hamrin Senorski, Eric,, Samuelsson, Kristian,   +2 more
core   +1 more source

Human evolution and the obstetrical dilemma: The pelvic floor hypothesis

The 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

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

Arthroscopy, 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, Su Yan, Pengcheng Tu, Xiaozhong Ma, Yunchen Wang, Hao Shu, Luning Sun   +6 more
wiley   +1 more source

Prevalence of celiac disease in children with joint hypermobility

, 2021
Introduction: Generalized joint hypermobility is a clinical feature that is associated with excessive joint laxity, which can occur alone or with various inherited disorders.
Sag, S., ÇAKIR, MURAT, KALYONCU, MUKADDES, GÜVEN, BURCU, Sag, E., DEMİR, FATMA   +5 more
core