Results 11 to 20 of about 2,781,607 (301)

Classification of congenital thumb hypoplasia and deformity

Chinese Journal of Plastic and Reconstructive Surgery, 2021
Background: Congenital thumb deformities account for one-third or more of all cases of congenital hand deformity. However, the current classification schemes of congenital thumb hypoplasia are no longer adequate due to their lack of adaptability to ...
Wei Wang, Chuanchang Dai, Lu Zhang
doaj   +2 more sources

Congenital hand anomalies in Upper Egypt

Indian Journal of Plastic Surgery, 2016
Background: Congenital hand anomalies are numerous and markedly variant. Their significance is attributed to the frequent occurrence and their serious social, psychological and functional impacts on patient’s life.
Tarek Abulezz, Mohamed Talaat, Asem Elsani, Karam Allam   +3 more
doaj   +2 more sources

Hand kinematics: Application in clinical practice

Indian Journal of Plastic Surgery, 2011
Pathological conditions of the hand consequent to injuries, paralysis, disease, arthritis and congenital difference results in loss or limitation of function, deformities, stiffness, inadequate power and poor position for pinch.
Santosh Rath
doaj   +4 more sources

The Impact of Microsurgery on Congenital Hand Anomalies Associated with Amniotic Band Syndrome

Plastic and Reconstructive Surgery, Global Open, 2018
Background:. Amniotic Band Syndrome is a clinical constellation of congenital anomalies characterized by constricting rings, tissue synechiae and amputation of body parts distal to the constriction bands.
David T. W. Chiu, MD, Anup Patel, MD, MBA, Sara Sakamoto, MD, Alice Chu, MD   +3 more
doaj   +2 more sources

“Less is More”- A Minimalistic Surgical Intervention to Correct the Right Upper Limb Deformity in an Isolated Right Radial Club Hand: A Case Report [PDF]

Journal of Orthopaedic Case Reports
Introduction: Radial club hand is a rare congenital condition (1 in 100,000) involving varying deformities on the radial side of the forearm, ranging from thumb underdevelopment to absence of the radius and related structures.
Sunil Kumar Rout, Mainak Mallik, Abhijit Kumar, Mandira Saha Mallik   +3 more
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Seropositive rheumatoid arthritis in osteogenesis imperfecta type XI (FKBP10 mutation): first case report and literature review [PDF]

Orphanet Journal of Rare Diseases
Background Osteogenesis imperfecta (OI) is a rare genetic disorder primarily caused by mutations in genes involved in type I collagen production. We report a 27-year-old female with genetically confirmed OI type XI (OI-XI) who experienced a delayed ...
Anas Manhal, Jamal Abdallah, Mahmoud M. Qouqas, Ahmad Waleed, Layth Al-Karaja, Noor Alhuda Sawalha, Laith Alamlih   +6 more
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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
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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
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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
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Prevalence of the Linburg-Comstock Anomaly in a Brazilian Population Sample [PDF]

Revista Brasileira de Ortopedia, 2020
Objective To determine the prevalence of the Linburg-Comstock anomaly in a Brazilian population sample. Methods A cross-sectional observational study was carried out between October 2017 and April 2018.
Leonardo Coêlho de Alencar Barreto, Carlos Henrique Fernandes, Luis Renato Nakachima, João Baptista Gomes dos Santos, Marcela Fernandes, Flavio Faloppa   +5 more
doaj   +3 more sources