1.
Rev. Soc. Boliv. Pediatr
;
54(2): 72-76, 2015. ilus
Article
in Spanish
| LILACS
| ID: lil-765406
ABSTRACT
Se presenta el caso clínico de un recién nacido con trombofilia hereditaria por deficiencia congénita de proteína C asociada a polimorfismo C677T del gen de la 5,10-metiltetrahidrofolato reductasa.
We present a clinical case of a newborn with inherited thrombophilia by congenital deficiency of protein C associated with the gene from the 5, 10-methyltetrahydrofolate reductase C677T polymorphism.