Results 31 to 40 of about 14,956 (269)

Interdigital neuroma in a patient with macrodactyly of the hallux

open access: yesJournal 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   +5 more
doaj   +1 more source

Foot Syndactyly: A Clinical and Demographic Analysis

open access: yesArchives 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   +2 more
doaj   +1 more source

Congenital tibial deficiencies: Treatment using the Ilizarov's external fixator [PDF]

open access: yes, 2009
SummaryIntroductionCongenital longitudinal deficiency of the tibia is a rare and often syndromic anomaly. Amputation is usually the preferred treatment option in complete absence of the tibia; however, a conservative management might be implemented in ...
Courvoisier, A.   +4 more
core   +61 more sources

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

open access: yesJournal 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   +6 more
doaj  

New Notations for Better Morphological Distinction of Postaxial Polydactyly of the Foot

open access: yesPlastic and Reconstructive Surgery, Global Open, 2022
Background:. There have been many reports on the classification and treatment of postaxial polydactyly of the foot. However, despite its being a common congenital anomaly, there is no universal notation about its morphology. Methods:.
Yuka Hirota, MD, PhD   +3 more
doaj   +1 more source

Arthrogryposis: A Rare Manifestation in Infant of Diabetic Mother [PDF]

open access: yes, 2009
Arthrogryposis multiplex congenita is characterized by non-progressive, multiple joint contractures present at birth. The major cause of arthrogryposis is fetal akinesia due to fetal abnormalities like neurogenic, muscle, connective tissue abnormalities ...
Kumar, Arvind   +2 more
core  

Lattice Structures for Bone Replacement: The Intersection of Bone Biomechanics, Lattice Design, and Additive Manufacturing

open access: yesAdvanced Materials Technologies, EarlyView.
This review outlines how understanding bone's biology, hierarchical architecture, and mechanical anisotropy informs the design of lattice structures that replicate bone morphology and mechanical behavior. Additive manufacturing enables the fabrication of orthopedic implants that incorporate such structures using a range of engineering materials ...
Stylianos Kechagias   +4 more
wiley   +1 more source

Management of the knees in arthrogryposis [PDF]

open access: yes, 2015
Arthrogryposis is defined as limited range of motion in three or more joints in two or more body parts. This article will describe treatment options for the arthrogrypotic knee.
Eva Pontén
core   +1 more source

Cellular Identity Crisis: RD3 Loss Fuels Plasticity and Immune Silence in Progressive Neuroblastoma

open access: yesAdvanced Science, EarlyView.
Researchers discovered that therapy‐induced loss of RD3 protein in neuroblastoma triggers a dangerous shift: cancer cells become more stem‐like, invasive, and resistant to treatment while evading immune detection. RD3 loss suppresses antigen presentation and boosts immune checkpoints, creating an immune‐silent environment.
Poorvi Subramanian   +7 more
wiley   +1 more source

Bilateral cleft foot: Radiographic and prenatal ultrasound features of two siblings with a review of literature

open access: yesMedicina, 2016
Cleft foot deformity, also known as ectrodactyly, is a rare congenital developmental defect of extremities caused by malformation in continuity of apical ectoderm.
Mehmet Sedat Durmaz   +5 more
doaj   +1 more source

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