Reconstructive surgery of rare upper limb congenital defects: 2 case reports
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F49777513%3A23310%2F14%3A43926978" target="_blank" >RIV/49777513:23310/14:43926978 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Reconstructive surgery of rare upper limb congenital defects: 2 case reports
Original language description
The main objective is to present two case reports of rare congenital differences of the upper extremity that belong to Category II of the modified classification of congenital hand deformities by Ogino et al. (1986). This classification was adopted by the Japanese Society for Surgery of the Hand in 1996. Category II includes incomplete formation of the joint, contracture and deformities due to failure of differentiation of parts and tumor-like conditions including hamartomas. Incomplete formation of thejoint may result in synostosis, congenital dislocation and ankylosis of digital joints.We present an individual comprehensive treatment of two children, Proximal radioulnar synostosis and ulnar hypoplasia in one and Partial ulnar aplasia associated withdislocation of radial head and humeroulnar synchrondrosis in the other.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FI - Traumatology and orthopaedics
OECD FORD branch
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Result continuities
Project
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Continuities
N - Vyzkumna aktivita podporovana z neverejnych zdroju
Others
Publication year
2014
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Pohybové ústrojí: Pokroky ve výzkumu, diagnostice a terapii
ISSN
1212-4575
e-ISSN
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Volume of the periodical
21
Issue of the periodical within the volume
3+4
Country of publishing house
CZ - CZECH REPUBLIC
Number of pages
21
Pages from-to
249-269
UT code for WoS article
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EID of the result in the Scopus database
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