Results 31 to 40 of about 12,205 (190)

Republication of “Current Concepts Review: Hallux Rigidus”

open access: yesFoot & Ankle Orthopaedics, 2023
Arthritis of the first metatarsophalangeal (MTP) joint, hallux rigid, is a common and disabling source of foot pain in the adult population. Hallux rigidus is characterized by diseased cartilage and large, periarticular osteophytes that result in a stiff,
Michael R. Anderson DO   +2 more
doaj   +1 more source

Hallux rigidus [PDF]

open access: yesJournal of Chiropractic Medicine, 2002
Hallux rigidus is a common problem of the first metatarsophalangeal joint and is particularly common in the 31-69 year old age group. Loss of articular cartilage narrowing of joint space and formation of periarticular osteophytes are present and increase over time, often leading to palpable osteophyte formation.
James W, Brantingham, Timothy G, Wood
openaire   +2 more sources

HALLUX RIGIDUS. [PDF]

open access: yesThe Lancet, 1900
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openaire   +2 more sources

Les exostoses de Turrett's: à propos de 35 cas

open access: yesThe Pan African Medical Journal, 2018
Nous rapportons à travers une étude rétrospective faite de 35 cas d’exostose sous unguéale de l’hallux dite exostose de Turrett's colligée entre 1995 et 2015 au service d’Orthopédie Traumatologie de l’Hôpital Militaire Principal d’Instruction de Tunis ...
Mounira Khezami   +5 more
doaj   +1 more source

Clinical Outcomes of Custom Foot Orthoses in Progressive Collapsing Foot Deformity: A Retrospective Cohort Analysis. [PDF]

open access: yesJ Foot Ankle Res
ABSTRACT Background Progressive collapsing foot deformity (PCFD) is a painful and function‐limiting condition most commonly affecting middle‐aged and older adults. Although custom foot orthoses (CFOs) are routinely prescribed as a conservative intervention, evidence from large clinical cohorts remains limited.
Robb K, Ryan M, Moisan G.
europepmc   +2 more sources

The Homozygous p.(Arg215Ter) Variant in XRCC2 Is Associated With Atypical Fanconi Anemia Without Major Hematological Abnormalities in Childhood

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli   +11 more
wiley   +1 more source

Epidemiology of hallux valgus surgery in Italy: A nationwide study from 2001 to 2016

open access: yesJournal of Experimental Orthopaedics
Purpose This study intended to estimate the annual number of hallux valgus surgical procedures in Italy and the patients' epidemiological features. A secondary goal was to compare the demographic differences in access to hallux valgus surgery amongst ...
Umile Giuseppe Longo   +10 more
doaj   +1 more source

Synovial Inflammation in Patients with Hallux Valgus is Similar to Changes Seen in Those with Hallux Rigidus

open access: yesFoot & Ankle Orthopaedics, 2022
Category: Basic Sciences/Biologics; Bunion Introduction/Purpose: Hallux valgus and hallux rigidus are common disorders that can have functional limitations for patients. Although both involve pathology centered around the first metatarsophalangeal joint (
Anthony L. Karzon   +5 more
doaj   +1 more source

Hallux Valgus [PDF]

open access: yesFoot & Ankle Orthopaedics, 2019
Hallux valgus is a common condition that results from a complex positional deformity of the first ray. The bunion or medial prominence that results from the lateral deviation and pronation of the hallux is only one component of the 3-dimensional deformity. Hallux valgus can lead to considerable pain and altered joint mechanics.
Justin J. Ray MD   +7 more
openaire   +3 more sources

Prenatal Evaluation of RNU4‐2 Variants in Fetuses With Central Nervous System Anomalies

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Fetal central nervous system (CNS) anomalies are among the most common congenital malformations, yet the overall prenatal diagnostic yield of current genetic testing remains below 40%. Variants in RNU4‐2, a non‐coding gene encoding the U4 small nuclear RNA (snRNA), have recently been linked to a novel highly recurrent dominant ...
Yiyao Chen   +13 more
wiley   +1 more source

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