Results 11 to 20 of about 83,420 (352)

Identification of Novel FBN2 Variants in a Cohort of Congenital Contractural Arachnodactyly

open access: yesFrontiers in Genetics, 2022
Congenital contractural arachnodactyly (CCA) is a rare autosomal dominant disorder of connective tissue characterized by crumpled ears, arachnodactyly, camptodactyly, large joint contracture, and kyphoscoliosis. The nature course of CCA has not been well-
Liying Sun   +38 more
doaj   +1 more source

Splinting Rheumatoid Hand Deformities: A Case Report

open access: yesAhi Evran Medical Journal, 2023
Rheumatoid arthritis (RA) is a disease of unknown origin characterized by inflammatory changes in the synovial tissue of joints, cartilage, and bone, and less frequently in extra-articular sites.
İsmail CEYLAN, Mehmet CANLI
doaj   +1 more source

Late reconstruction of a traumatized hand with loss of multiple fingers [PDF]

open access: yesRevista Brasileira de Cirurgia Plástica, 2017
Mutilating hand injuries are a challenge to both the hand surgeon and the patient. The surgeon must make decisions ranging from the initial debridement to which fingers and joints will be preserved and the appropriate use of the parts to be removed. Late
Renan Lyuji Takemura   +5 more
doaj   +1 more source

Grinder Injury of the Hand: A Rare but Devastating Occupational Hazard

open access: yesThe Surgery Journal, 2021
Food handlers and workers are exposed to several occupational hazards not frequented by the general population. Grinder injuries of the hand present a devastating consequence of industrial food processing that is infrequently described.
Tushar Patial   +4 more
doaj   +1 more source

Hand deformities in Parkinsonism [PDF]

open access: yesJournal of Chronic Diseases, 1965
Abstract In a series of 86 patients with Parkinsonism there were 34 (40 per cent) who had some deformity of the hands. These deformities occurred more frequently among those with post-encephalitic Parkinsonism than in those who gave no history of encephalitis.
Reynolds, Frank W.   +1 more
openaire   +3 more sources

Analysis of factors influencing postoperative hand function in DEB with hand deformities

open access: yesPifu-xingbing zhenliaoxue zazhi, 2021
Objective: To investigate the influencing factors of postoperative hand function in patients with dystrophic epidermolysis bullosa. Methods: A retrospective analysis was performed in 41 patients with dystrophic epidermolysis bullosa with hands ...
Xinhe JIAO, Yuluo JIAN, Lu WANG
doaj   +1 more source

Baller-Gerold Syndrome in a Premature Infant with a Mutation in the RECQL4 Gene [PDF]

open access: yesNeonatal Medicine, 2019
Baller-Gerold syndrome is a rare autosomal recessive disorder characterized by premature fusion of the cranial sutures and malformation of the upper limb extremities at birth.
Ji Sook Kim
doaj   +1 more source

Novel genetic syndrome manifesting with cerebral atrophy, cataract, hypoacusis, diabetes, and brachy-/syndactyly

open access: yesJournal of Family Medicine and Primary Care, 2023
Genetic disorders manifest clinically in a variety of phenotypes. A patient with cataract, hypoacusis, hand and foot deformities, and diabetes was not reported.
Josef Finsterer
doaj   +1 more source

Pre-operative scrutiny of late burned hand presentations: Crucial step for the improvement of results

open access: yesBurns Open, 2021
Post burn contractures are a common occurrence after severe burn injuries. In more than 80% of all burns, the hand is involved (Fufa et al., 2014). This article aims to emphasize on the need of detailed pre-operative scrutiny of hand deformities and ...
Veena Singh   +5 more
doaj   +1 more source

Surgical management of hand deformities in hereditary dystrophic epidermolysis bullosa [PDF]

open access: yesVojnosanitetski Pregled, 2003
In the period 1996-2001 in the Clinic for Plastic Surgery and Burns of the Military Medical Academy, 18 patients. 12 male and 6 female, with hereditary dystrophic epidermolysis bullosa (HDEB) and hand deformities were surgically treated, to achieve the ...
Panajotović Ljubomir   +2 more
doaj   +1 more source

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