Warfarin embryopathy;Fœtopathie coumarinique

Archives de Pediatrie

Volumn 9, Issue 7, 2002, Pages 705-708

  Bony, C ^a   Zyka, F ^a   Tiran Rajaofera, I ^a   Attali, T ^a   De Napoli, S ^a   Alessandri, J L ^a  

^a Centre Hospitalier Departemental Felix Guyon   (France)

Author keywords

Chondrodysplasia punctata; Fetal diseases; Infant, newborn; Prenatal exposure delayed effects; Warfarin

Indexed keywords

ACENOCOUMAROL; ANTIVITAMIN K; WARFARIN; ANTICOAGULANT AGENT;

ARTICLE; CASE REPORT; CATARACT; CHONDRODYSPLASIA PUNCTATA; CLINICAL FEATURE; DISEASE COURSE; DRUG METABOLISM; EMBRYOPATHY; FACE DYSMORPHIA; HUMAN; INFANT; PRENATAL EXPOSURE; VALVULAR HEART DISEASE; WARFARIN EMBRYOPATHY; ADULT; AGE; CHEMICALLY INDUCED DISORDER; COMPARATIVE STUDY; CONGENITAL MALFORMATION; DRUG EFFECT; FEMALE; FETUS; FOLLOW UP; HEART VALVE PROSTHESIS; MALE; PREGNANCY; PREGNANCY COMPLICATION; PRESCHOOL CHILD; TIME;

ABNORMALITIES, DRUG-INDUCED; ACENOCOUMAROL; ADULT; AGE FACTORS; ANTICOAGULANTS; CHILD, PRESCHOOL; CHONDRODYSPLASIA PUNCTATA; FEMALE; FETUS; FOLLOW-UP STUDIES; HEART VALVE PROSTHESIS; HUMANS; INFANT; MALE; PREGNANCY; PREGNANCY COMPLICATIONS, CARDIOVASCULAR; PRENATAL EXPOSURE DELAYED EFFECTS; TIME FACTORS; WARFARIN;

EID: 0036067990     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0929-693X(01)00970-8     Document Type: Article

References (8)

1. Maternal and fetal sequelae of anticoagulation during pregnancy
2. Anticoagulation of pregnant women with mechanical heart valves
3. Chondrodysplasia punctata: A boy with X-linked recessive chondrodysplasia punctata due to an inherited X-Y translocation with a current classification of these disorders
4. Une nouvelle arylsulfatase á l'origine de la chondrodys-plasie ponctuée récessive liée á l'X et peut-être d'une embryopathie médicamenteuse
5. Vitamin K deficiency embryopathy: A phenocopy of the warfarin embryopathy due to a disorder of embryonic vitamin K metabolism
6. Association of congenital deficiency of multiple vitamin K-dependant coagulation factors and the phenotype of the warfarin embryopathy: Clues to the mechanism of teratogenicity of coumarin derivatives
7. Mechanism of bone and cartilage maldevelopment in the warfarin embryopathy
8. Mutations in the gene encoding the human matrix Gla protein cause Keutel syndrome