Results 31 to 40 of about 598,158 (213)

Foot Syndactyly: A Clinical and Demographic Analysis

Archives of Plastic Surgery, 2016
Background Syndactyly of the foot is the second most common congenital foot anomaly. In East Asia, however, no large case study has been reported regarding the clinical features of isolated foot syndactyly.
Jong Ho Kim, Byung Jun Kim, Sung Tack Kwon   +2 more
doaj   +1 more source

A distinctive presentation of diplopodia: a Y-metatarsal combining the extra foot and the extra digit of the main foot.

, 2013
Diplopodia is a rare congenital anomaly and has been described as extra digits, metatarsals, and tarsal bones that form an extra foot or foot-like structure.
Hocaoglu, Emre, Berkoz, Omer, Ozkan, Turker, Dogan, Yunus   +3 more
core   +1 more source

A Case of Macrodystrophia Lipomatosa of the Lower Extremity: An Effective Measuring of the Dynamic Plantar Pressure for Severe Congenital Deformity

Journal of Plastic and Reconstructive Surgery, 2022
Macrodystrophia lipomatosa is a rare, congenital, non-hereditary form of localized gigantism characterized by abnormal fibroadipose tissue proliferation.
Kenta Ikushima, Yoshiro Abe, Hiroyuki Yamasaki, Yutaro Yamashita, Shinji Nagasaka, Masahiro Takaiwa, Ichiro Hashimoto   +6 more
doaj  

Neurological, Neurodevelopmental and Treatment Outcomes in Patients With Pyruvate Dehydrogenase Complex Deficiency

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective The aim of this study was to characterize intellectual and motor function, neurological features including epilepsy, treatment response, and adaptive behavior in patients with pyruvate dehydrogenase complex deficiency (PDCD) in Sweden.
Antri Savvidou, Colin Reilly, Kalliopi Sofou, Sofia Ygberg, Erik A. Eklund, Karin Naess, Niklas Darin   +6 more
wiley   +1 more source

Interdigital neuroma in a patient with macrodactyly of the hallux

Journal of the Foot & Ankle, 2020
A patient with macrodactyly of the hallux, returned 2 years after amputation of the distal phalanx, complaining of pain and swelling in the plantar foot. The Tinel, Moulder, and Gauthier signs were all present.
Henrique Santos Barbosa da Silva, Luiz Carlos Ribeiro Lara, Lucio Carlos de Azevedo Torres Filho, Fabio Lemos Rodrigues, Juan Antonio Grajales, Lara Furtado Lancia   +5 more
doaj   +1 more source

PIE BOT: CONCEPTOS ACTUALES

Revista Médica Clínica Las Condes, 2021
Resumen: El pie bot es la deformidad congénita más frecuente de las extremidades inferiores del ser humano, afectando a 1 de cada 1000 recién nacidos vivos.
Estefanía Birrer, Macarena Morovic, Pablo Fernández   +2 more
doaj   +1 more source

TH/TRs–COL11A2 Axis Mediates Loss of a Differentiated Astrocyte State in Hypogyrified Brains

Advanced Science, EarlyView.
Using a gyrencephalic congenital hypothyroidism pig model, this study reveals cerebral atrophy and cortical hypogyrification. Single‐cell sequencing identifies astrocytes as major TH‐responsive cells, with the COL11A2‐enriched Astro‐2 state nearly absent.
Ying Zhang, Xiao Wang, Hongyan Ma, Pengcheng Lyu, Shuangjie Tian, Ruojun Zong, Jiani Chen, Gang Ren, Yongjiang Yang, Zichen Yang, Guosong Qin, Naishi Li, Yanfang Wang, Jianwei Jiao, Jianguo Zhao   +14 more
wiley   +1 more source

Treatment of congenital deformities of cleft foot and syndactyly: A case report and review of the literature

Turkish Journal of Plastic Surgery
Cleft foot is a rare congenital anomaly characterized by a central conical defect and deficiency of the foot rays. Syndactyly is the fusion of the skin with or without the bone of adjacent digits, and it may be associated with syndrome-related cleft foot.
Nuh Evin, Yasir Vural, Can Koç, Gökçer Uzer   +3 more
doaj   +1 more source

Pattern of Congenital Musculoskeletal Deformities at the State Hospital, Abeokuta, South-West Nigeria

, 2009
Background: Congenital anomalies are recognisable causes of disability in developed and developing countries. 2-4% of newborns worldwide have congenital anomalies affecting various systems including the musculoskeletal system. The incidence of congenital
Aigoro, NF, Popoola, M, Oloko, M
core   +1 more source

A Spatiotemporal Single‐Cell Atlas Uncovers Dysregulated ECM Dynamics and Septal Remodeling Arrest in Human Ventricular Septal Defects

Advanced Science, EarlyView.
Integrating single‐cell and spatial transcriptomics reveals human ventricular septal defect (VSD) as a disease of microenvironmental insufficiency and structural remodeling arrest. Attenuated endothelial‐fibroblast crosstalk, alongside downregulated THBS1/TGF‐β1 and MMP2 signaling networks, impairs the endothelial‐to‐mesenchymal transition (EndoMT) and
Xiaoyuan Zhang, Lun Zhu, Ze Sun, Ruolin Jia, Ziming Wang, Jiayao Zhao, Bohao Liu, Haiqing Xiong, Xiaowei Yu, Yanzhu Yue   +9 more
wiley   +1 more source