Ocular and Systemic Findings in COL2A1 and COL11A1 Stickler Syndrome
ABSTRACT Stickler syndrome is most commonly caused by variants in COL2A1 and COL11A1 genes. The purpose of this study was to describe genetic variants and phenotypes in COL2A1 and COL11A1 Stickler syndrome. We performed a retrospective genotype–phenotype evaluation of COL2A1 and COL11A1 Stickler syndrome subjects. Thirty‐two subjects with COL2A1 and 13
Aileen G. MacLachlan +5 more
wiley +1 more source
Comparing kinematic and kinetic demands on the knee joint during selected physiotherapy exercises and activities of daily living. [PDF]
Gschoßmann L +5 more
europepmc +1 more source
ABSTRACT Detailed clinical phenotypes have been previously reported for 33 individuals with X‐linked HNRNPH2‐related neurodevelopmental disorder. Of these, 75% self‐reported a musculoskeletal abnormality, including hip dysplasia, scoliosis, kyphosis, lordosis, pes planus, arthritis, and missing spinous processes.
Ambar Garcia +6 more
wiley +1 more source
Interleukin-33-Mediated Mechanical-Loading Induced Degeneration of Knee Joint Chondrocytes. [PDF]
Zhang J +5 more
europepmc +1 more source
ABSTRACT Dengue virus (DENV) poses a serious global health challenge, particularly in cases of dengue hemorrhagic fever (DHF). Patients with preexisting mitochondrial disorders may be at increased risk for complications due to the specific impact of DENV on mitochondrial‐dependent cellular processes and immune function.
Audra N. Iness +11 more
wiley +1 more source
Proximal tibial tuberculous osteomyelitis with secondary knee joint arthritis: A case report. [PDF]
Haichour I +3 more
europepmc +1 more source
Characterization and Analysis of PHEX Variants in Patients With Hypophosphatemia in Argentina
ABSTRACT Confirming the underlying molecular etiology of hereditary hypophosphatemia (HH) to provide recurrence risk counseling is highly important. Our aims were to describe the detected variants and their distribution across Argentina and to contrast them with published data.
Silvia Ávila +3 more
wiley +1 more source
Correction: Correlation study: electrical impedance-based approximation of knee joint angle and extensor strength during concentric knee extension. [PDF]
Thönes JP +5 more
europepmc +1 more source
The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome
ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley +1 more source
Development of a knee joint magnetic resonance imaging (MRI)-based model for finite element analysis (FEA) applications. [PDF]
Vasiliadis AV +7 more
europepmc +1 more source

