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Caudal regression syndrome in one of dizygotic twins
Z. Krenova, L. Elstnerova, Z. Dolezel, L. Kren
Language English Country England, Great Britain
Document type Case Reports, Journal Article, Twin Study
- MeSH
- Digestive System Abnormalities genetics pathology MeSH
- Anal Canal abnormalities pathology MeSH
- Twins, Dizygotic MeSH
- Sacrum abnormalities pathology MeSH
- Humans MeSH
- Infant, Newborn MeSH
- Rectum abnormalities pathology MeSH
- Syringomyelia genetics pathology MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Infant, Newborn MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Twin Study MeSH
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.
Department of Pathology University Hospital Brno Czech Republic
Department of Pediatric Oncology University Hospital Brno Czech Republic EU
Department of Pediatrics University Hospital Brno Czech Republic
References provided by Crossref.org
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