Antepartum findings in fetal protein C deficiency
β Scribed by P. Kirkinen; M. Salonvaara; K. Nikolajev; R. Vanninen; K. Heinonen
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 161 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0197-3851
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract A rare association of congenital afibrinogenemia and hereditary protein C deficiency is described in a 37βyearβold female who suffered from ischemic necrosis in the left first toe. The diagnosis of afibrinogenemia was assessed by the absence of fibrinogen in clotting and immunological a
We report the ultrasound, cytogenetic and morphologic findings in a case of trisomy 10 mosaicism prenatally detected by chorionic villus sampling (CVS). CVS sampling was carried out at the 13th week of gestation because of ultrasound diagnosis of hydrops fetalis and hygroma colli. Trisomy 10 mosaici