Amouzou KS, Malonga-Loukoula ELJ, Kouevi-Koko TE, Bakriga B, Abalo A. Foot hexadactyly, social implications and management in the African setting: Case report. Turk J Pediatr 2018; 60: 453-455. Hexadactyly of the foot, an abnormal congenital condition presenting as eight toes, is a rare malformation. We report the case of a ten-year-old girl, admitted to our orthopedic and reconstructive surgery department for a preaxial hexadactyly. The girl was abandoned by her parents at birth and stopped school early due to stigmatization. The goals of the surgical procedure were: social reintegration, gait improvement, ability to wear shoes comfortably, and improved appearance of the foot. The surgery was a medial resection of the supernumerary toes.
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http://dx.doi.org/10.24953/turkjped.2018.04.018 | DOI Listing |
Int J Mol Sci
July 2024
Dipartimento di Oncologia e Medicina Molecolare, Istituto Superiore di Sanità, 00161 Rome, Italy.
Cureus
April 2023
Paediatrics, Military Hospital Ambala, Ambala, IND.
Heptadactyly and hexadactyly are rare congenital disorders from the polydactyly family. This type of polydactyly is usually classified into three major groups: preaxial (medial ray), postaxial (lateral ray), and central polydactyly. The most common presentation is both preaxial and postaxial polydactyly.
View Article and Find Full Text PDFGenomics
July 2021
Medical Genomics Research Department, King Abdullah International Medical Research Center (KAIMRC), King Saud bin Abdulaziz University for Health Sciences, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia; Division of Genetics, Department of Pediatrics, King Abdullah Specialized Children's Hospital, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Polydactyly or hexadactyly is characterized by an extra digit/toe with or without a bone. Currently, variants in ten genes have been implicated in the non-syndromic form of polydactyly. DNA from a single affected individual having bilateral postaxial polydactyly was subjected to whole exome sequencing (WES), followed by Sanger sequencing.
View Article and Find Full Text PDFActa Med Okayama
October 2020
Department of Pediatrics, Okayama University Hospital, Okayama 700-8558, Japan.
Polydactyly is one of the most common foot congenital anomalies. It is often detected immediately after birth, but the diagnosis can sometimes be delayed if the symptoms are less evident. A 2-year-old girl with a complaint of recurrent bleeding from the right toenail was diagnosed with foot polydactyly.
View Article and Find Full Text PDFExp Mol Pathol
August 2020
University of Pecs, Medical School, Department of Medical Genetics, Pecs, Hungary; Szentagothai Research Center, University of Pecs, Pecs, Hungary.
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus (MPPH) syndrome is a developmental brain disorder characterized by an enlarged brain size with bilateral perisylvian polymicrogyria and a variable degree of ventriculomegaly. MPPH syndrome is associated with oromotor dysfunction, epilepsy, intellectual disability and postaxial hexadactyly. The molecular diagnosis of this disorder is established by the identification of a pathogenic variant in either AKT3, CCND2 or PIK3R2.
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