Results 11 to 20 of about 1,742 (244)

Surgical treatment of hand deformities in multiple enchondromatosis: a case report

Acta Orthopaedica et Traumatologica Turcica, 2021
Multiple enchondromatosis (Ollier’s disease) is a rare disease characterized by widespread enchondromas. In general, the short tubular bones of the hand are involved, with progressive lesions resulting in cosmetic problems and functional deformities ...
Bulent Erol, Cihangir Tetik, Evrim Sirin, Baris Kocaoglu, Murat Bezer   +4 more
doaj   +1 more source

Cleft hand classification and treatment: literature review [PDF]

Revista Brasileira de Cirurgia Plástica, 2022
Cleft hand is a rare congenital deformity characterized by a longitudinal deficiency of the central rays of the hand, which may be associated with other malformations. Due to the wide spectrum of manifestations, the treatment is challenging.
André Gustavo Pontes de Carvalho Pires, Marcela dos Santos Martins, João Carlos Nakamoto, Marcos Marcatto Abreu, Renato Novaes Oliveira, Arthur Perez Ferreira   +5 more
doaj   +1 more source

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

Frontiers 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, Yingzhao Huang, Yingzhao Huang, Yingzhao Huang, Sen Zhao, Sen Zhao, Sen Zhao, Wenyao Zhong, Jile Shi, Jile Shi, Jile Shi, Yang Guo, Junhui Zhao, Ge Xiong, Yuehan Yin, Zefu Chen, Zefu Chen, Zefu Chen, Nan Zhang, Zongxuan Zhao, Qingyang Li, Dan Chen, Yuchen Niu, Yuchen Niu, Xiaoxin Li, Xiaoxin Li, Guixing Qiu, Guixing Qiu, Guixing Qiu, Zhihong Wu, Zhihong Wu, Zhihong Wu, Terry Jianguo Zhang, Terry Jianguo Zhang, Terry Jianguo Zhang, Wen Tian, Nan Wu, Nan Wu, Nan Wu   +38 more
doaj   +1 more source

Hand Deformities in Rheumatoid Disease [PDF]

Annals of the Rheumatic Diseases, 1957
D A Brewerton
exaly   +3 more sources

Evaluation of Non-coverage Cost Effective Technique for Management of Epidermolysis Bullosa Mitten Hands in Developing Countries

Egyptian Journal of Plastic and Reconstructive Surgery, 2021
Background: Epidermolysis bullosa (EB) is a group of rare genetic disorders known by susceptibility of the skin epidermis and mucosa that separate from underlying tissues and cause increase in skin fragility, blistering, and scarring in response to minor
adel sayed amr, Omar Mahmoud, Mohamed Ghanem   +2 more
doaj   +1 more source

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

Revista 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, Hugo Alberto Nakamoto, Fernanda do Carmo Iwase, João Carlos Nakamoto, Bruno Azevedo Veronesi, Teng Hsiang Wei   +5 more
doaj   +1 more source

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

Pifu-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

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

The 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, Rajinder K. Mittal, Ramneesh Garg, Sheerin Shah, Amandeep Kaur   +4 more
doaj   +1 more source

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

Neonatal 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

Journal 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