Cadual regression syndrome in one of dizygotic twins.

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F10%3A00051736" target="_blank" >RIV/00216224:14110/10:00051736 - isvavai.cz</a>

Result on the web

<a href="http://dx.doi.org/10.3109/15513815.2010.505629" target="_blank" >http://dx.doi.org/10.3109/15513815.2010.505629</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.3109/15513815.2010.505629" target="_blank" >10.3109/15513815.2010.505629</a>

Result language

angličtina

Original language name

Cadual regression syndrome in one of dizygotic twins.

Original language description

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.

Czech name

—

Czech description

—

Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

FG - Paediatrics

OECD FORD branch

—

Project

—

Continuities

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year

2010

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Fetal and Pediatric Pathology

ISSN

1551-3815

e-ISSN

—

Volume of the periodical

29

Issue of the periodical within the volume

6

Country of publishing house

US - UNITED STATES

Number of pages

5

Pages from-to

419-423

UT code for WoS article

000283736600008

EID of the result in the Scopus database

—