KŘENOVÁ, Zdenka, Lia ELSTNEROVÁ, Zdeněk DOLEŽEL and Leoš KŘEN. Cadual regression syndrome in one of dizygotic twins. Fetal and Pediatric Pathology. USA: TAYLOR & FRANCIS, 2010, vol. 29, No 6, p. 419-423. ISSN 1551-3815. Available from: https://dx.doi.org/10.3109/15513815.2010.505629.
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Basic information
Original name Cadual regression syndrome in one of dizygotic twins.
Authors KŘENOVÁ, Zdenka (203 Czech Republic, guarantor, belonging to the institution), Lia ELSTNEROVÁ (203 Czech Republic, belonging to the institution), Zdeněk DOLEŽEL (203 Czech Republic, belonging to the institution) and Leoš KŘEN (203 Czech Republic, belonging to the institution).
Edition Fetal and Pediatric Pathology, USA, TAYLOR & FRANCIS, 2010, 1551-3815.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30209 Paediatrics
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 0.404
RIV identification code RIV/00216224:14110/10:00051736
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.3109/15513815.2010.505629
UT WoS 000283736600008
Keywords in English TERMINAL DELETION; SACRAL AGENESIS; MODEL
Tags International impact
Changed by Changed by: Mgr. Michal Petr, učo 65024. Changed: 20/4/2012 11:36.
Abstract
Caudal regression syndrome is a rare congenital condition characterized by varying degrees of developmental failure ranging from a partial sacral agenesis to the absence of lumbosarcal spine, hypoplasia, or fusion of the lower extremities and visceral anomalies. This is the third case of only one of the twins involved by this syndrome described in the literature and the second case of the selective involvement in dizygotic twins. Selective involvement of only one twin suggests that factors other than hyperglycemia and 7q deletions may be involved in the pathogenesis.
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