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Congenital Anomalies of the Hand: A Clinical Study

Hahn SB, Kang ES, Park BM, Ahn EH

Congenital hand anomalies encompass a very broad spectrum of deformity, and precise classification of these deformities has always posed a major problem. We reviewed 50 cases of congenital hand deformities...
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An autopsy case of Adams-Oliver syndrome

Jun SY, Khang SK, Park SH

We report an autopsy case of a male fetus with Adams-Oliver syndrome. His mother was a healthy, 31-year-old woman and her family and past histories were unremarkable. Therapeutic termination was...
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Congenital Differences of the Upper Extremity: Classification and Treatment Principles

Chung MS

For hand surgeons, the treatment of children with congenital differences of the upper extremity is challenging because of the diverse spectrum of conditions encountered, but the task is also rewarding...
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A Case of Schinzel-Giedion Syndrome

Park KH, Hwang SH, Byun SY

Schinzel-Giedion syndrome (SGS) is a rare malformation syndrome characterized by severe midface retraction, multiple congenital malformations including hydronephrosis, congenital heart defect, skeletal anomalies and hypertrichosis, and a higher prevalence of...
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Free Fat Graft for Congenital Hand Differences

Ogino T, Ishigaki D, Satake H, Iba K

BACKGROUND: Free fat graft has been used for the treatment of congenital hand differences. However, there have been a few reports about the outcome of that treatment. In this study,...
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Changing Paradigms in the Treatment of Radial Club Hand: Microvascular Joint Transfer for Correction of Radial Deviation and Preservation of Long-term Growth

de Jong JP, Moran SL, Vilkki SK

Radial longitudinal deficiency, also known as radial club hand, is a congenital deformity of the upper extremity which can present with a spectrum of upper limb deficiencies. The typical hand...
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Pollicization: The Concept, Technical Details, and Outcome

Kozin SH

Pollicization substitutes a functioning finger for a deficient thumb. The most indication is thumb hypoplasia with absence or instability of the carpometacarpal joint. However, there are additional causes that may...
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In Silico Study of Human Gap Junction Beta-2 Protein by Homology Modeling

Shehzadi A, Masood K

  • KMID: 2166480
  • Genomics Inform.
  • 2010 Jun;8(2):70-75.
Asp66his, Asp54Lys, and Asp50Asn are mutations in connexin 26 that are observed in the clinic and give rise to autosomal dominant syndromes. They are the result of point mutations in...
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Thumb Duplication: Concepts and Techniques

Tonkin MA

Within the Oberg, Manske, Tonkin (OMT) classification, thumb duplications are a failure of formation and/or differentiation affecting the radial-ulnar axis of the hand plate. The Wassel description of seven types...
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A Case of Weill-Marchesani Syndrome with Inversion of Chromosome 15

Chung JL, Kim SW, Kim JH, Kim TI, Lee HK, Kim EK

PURPOSE: To present a case of Weill-Marchesani syndrome with corneal endothelial dysfunction due to anterior dislocation of a spherophakic lens and corneolenticular contact. METHODS: A 17-year-old woman presented...
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