Deficiencia congénita de Proteína C asociada a polimorfismo C677T del gen de la 5,10-metiltetrahidrofolato reductasa, a propósito de un caso / Congenital deficiency of protein C associated with C677T polymorphism of the gene from the 5,10-methyltetrahydrofolate reductase. Case report
Rev. Soc. Boliv. Pediatr
;
54(2): 72-76, 2015. ilus
Article
in Spanish
| LILACS
| ID: lil-765406
RESUMEN
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.
ABSTRACT
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.
Full text:
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Index:
LILACS (Americas)
Type of study:
Risk factors
Language:
Spanish
Journal:
Rev. Soc. Boliv. Pediatr
Journal subject:
Pediatrics
Year:
2015
Type:
Article
Affiliation country:
Bolivia
Institution/Affiliation country:
Hospital del Niño Dr. Ovidio Aliaga Uría/BO
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