نتایج جستجو برای: polydactyly

تعداد نتایج: 1218  

2007
Bianca Carstanjen Marie Abitbol Christophe Desbois

The following case report describes the diagnosis and surgery of bilateral polydactyly of unknown origin in a colt. A 7-month-old Berber colt was referred for cosmetic and curative excision of supernumerary digits. Radiographic examination revealed bilateral polydactyly and welldeveloped first carpal bones. Surgery consisted of an osteotomy of both second metacarpal bones combined with an amput...

2015
Kewal Arunkumar Mistry Rohit Bhoil Ankitkumar Patel

Joubert's syndrome is indeed a rarity in clinical and radiological practice with a myriad of accompanying anomalies. Figure 1. Clinical photos of the patient showing post-axial polydactyly in the upper and lower limbs (A, B) and broad flat nasal bridge (C). Herein we present a case of an eight-month-old female infant who presented with delayed milestones, nystagmus and post-axial polydactyly (F...

Journal: :Radiology Case Reports 2019

Journal: :Journal of Hand Surgery 1993

Journal: :Indian Journal of Dermatology, Venereology, and Leprology 2010

2014
Alireza Jalili Farid Najd Mazhar

Radial polydactyly, the most common digital duplication in Asian and white populations, has a wide range of manifestations. Its classification is useful for planning and assessing surgical treatment. Our patient had four thumbs, duplicated radial carpal bones, and a bifurcated radius. This presentation is not covered by any of the current classifications. To the best of our knowledge, this is t...

Journal: :Journal of medical genetics 1994
C Wright R Healicon C English J Burn

Two sibs are described, the first of whom presented the classic Meckel syndrome triad of encephalocele, postaxial polydactyly, and characteristic renal cystic changes. The second sib had none of these abnormalities, but did show urethral atresia and preaxial polydactyly, two features previously described in some patients with Meckel syndrome. The two cases illustrate both the wide phenotypic sp...

2004
Sukru Ulusoy Kubra Kaynar Semih Gul Kubilay Ukinc

Objective: To describe a case of Bardet-Biedl syndrome involving renal failure and retinal dystrophy. Case Presentation and Intervention: A 50-year-old female patient presented to the emergency service with uremic symptoms and metabolic acidosis. Polydactyly, retinitis pigmentosa, obesity, strabismus, nistagmus and renal failure were found. Because she had end-stage renal failure, hemodialysis ...

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