Bilateral toe syndactyly – short review based on a case report [PDF]
Romanian Journal of Medical Practice, 2021 Non-syndromic toe syndactyly is a regular cause of foot malformation in children, bilateral form being less common. Syndactyly release procedures had few contraindications, as uncomplicated malformation or important patient comorbidities.
Tiberiu Paul Neagu +2 more
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Resolution of 2nd, 3rd or 4th interdigital space incomplete, simple syndactyly using a random vascularity flap [PDF]
Plastic and Aesthetic Research, 2017 Syndactyly consists of a variable fusion of soft tissue or of bone in adjacent fingers. This has important aesthetic and functional impacts on the development of the child due to the abnormal appearance of the hand. When the 1st web space is affected, it
Alejandro Angel Corona Figueroa
exaly +6 more sources
Four Unusual Cases of Congenital Forelimb Malformations in Dogs [PDF]
Animals, 2021 Four dogs were presented with thoracic limb deformity. After clinical and radiographic examinations, a diagnosis of congenital malformations was performed for each of them.
Simona Di Pietro +6 more
doaj +2 more sources
Surgical results from treating children with syndactyly through the collective effort system at "SOS Hand Recife" between 2005 and 2009 [PDF]
Revista Brasileira de Ortopedia, 2014 Objective:to evaluate the results from and parents' satisfaction with treatment for children with syndactyly who were operated at the "SOS Hand Recife" hospital between 2005 and 2009.Methods:data for assessing the results were gathered from the patients'
Mauri Cortez +6 more
doaj +2 more sources
Unilateral syndactyly, hemihypertrophy, and hyperpigmentation with mosaic 2q35 deletion [PDF]
Indian Journal of Dermatology, 2023 Pigmentary mosaicism (PM) is a clinical condition of dyspigmentation with chromosomal abnormality. PM presents with both cutaneous and extracutaneous manifestation. Hypomelanosis of Ito and linear and whorled nevoid hypermelanosis are syndromic disorders
Akhtar Ali +4 more
doaj +2 more sources
Principles of surgical treatment in patients with complicated syndactyly [PDF]
Acta Orthopaedica et Traumatologica Turcica, 2021 Methods: Thirteen patients (10 females, 77%; 3 males, 23%) underwent surgery for congenital complicated syndactyly. Mean age of operation was 6.3 years (range 0.5-21 years). Four patients had bilateral syndactyly.
Emre Orhun +4 more
doaj +1 more source
New simple technique for syndactyly separation [PDF]
, 2020 Objectives/Interrogation: Web reconstruction in finger syndactyly using a hexagonal dorsal skin flap and a straight midline incision gives a good cosmetic and functional result with little need for skin grafts. Methods: We developed an easy technique to be used in simple complete (SC), simple[for full text, please go to the a.m. URL]
Nietosvaara, Y, Grahn, P, Sommarhem, A
openaire +3 more sources
SURGICAL TECHNIQUE FOR COMPLEX SYNDACTYLY IN APERT SYNDROME: A SERIAL CASE [PDF]
Jurnal Rekonstruksi dan Estetik, 2019 Highlights: • Complex syndactyly in Apert syndrome, particularly when complicated with synonychia and synostosis, poses a significant surgical challenge.
Williams Mesang +2 more
doaj +3 more sources
POST-OPERATIVE SIMPLE INCOMPLETE ACQUIRED SYNDACTYLY IN THIRD AND FOURTH DIGITI MANUS SINISTRA: A CASE REPORT [PDF]
Jurnal Widya MedikaSyndactyly is interdigiti soft tissue and/or osseous fusion or adhesion and may affect hand and/or foot. Syndactyly is caused by congenital or acquired. Acquired syndactyly is a rare disease that may caused by trauma, inflammation, or infection around the finger. This abnormality may affect aesthetic and functional impairment, so that surgery procedure
Evita Zevanya, Samuel Zacharias
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Outcomes of V-Y Dorsal Metacarpal Artery Perforator Flap for Web Space Reconstruction in Simple Syndactyly [PDF]
Egyptian Journal of Plastic and Reconstructive SurgeryBackground: New web space formation is the most challengingin the treatment of syndactyly, and the choice of theideal reconstructive technique is still controversial.
Ahmed Bahaa El Din +3 more
doaj +2 more sources