1.
J Pediatr
; 134(6): 777-9, 1999 Jun.
Article
in English
| MEDLINE
| ID: mdl-10356151
ABSTRACT
Prothrombin G20210A is a newly described common mutation that is associated with an increased risk of arterial and venous thrombosis. We describe a healthy child heterozygous for this prothrombin mutation who had a spinal cord infarct with no other prothrombotic risk factors.
Subject(s)
Infarction/genetics , Mutation , Prothrombin/genetics , Spinal Cord/blood supply , Family , Female , Heterozygote , Humans , Infant , Infarction/diagnosis , Infarction/therapy , Magnetic Resonance Imaging , Risk Factors , Thrombophilia/genetics
2.
J Pediatr
; 88(6): 989-90, 1976 Jun.
Article
in English
| MEDLINE
| ID: mdl-1271201