1.
J Pediatr Hematol Oncol
; 42(6): e511-e512, 2020 08.
Artículo
en Inglés
| MEDLINE
| ID: mdl-30870385
RESUMEN
Factor X deficiency is a severe inherited coagulation disorder, which is characterized by severe systemic bleeding manifestations in affected individuals. It is a rare disorder with a frequency of around 1:1,000,000 in the general population. We present the case of an infant with factor X deficiency who presented with complex febrile seizure. Although febrile seizures are very common in children, a closer scrutiny leads to neuroimaging and finding of intracranial bleed. Hematologic and genetic investigations confirmed the diagnosis. A high index of suspicion should be maintained to diagnose uncommon bleeding disorders in children.
Asunto(s)
Deficiencia del Factor X/diagnóstico , Hemorragias Intracraneales/diagnóstico , Neuroimagen/métodos , Convulsiones Febriles/diagnóstico , Diagnóstico Diferencial , Deficiencia del Factor X/diagnóstico por imagen , Humanos , Lactante , Hemorragias Intracraneales/diagnóstico por imagen , Masculino , Pronóstico , Convulsiones Febriles/diagnóstico por imagen
2.
J Neuroimmunol
; 328: 76-77, 2019 03 15.
Artículo
en Inglés
| MEDLINE
| ID: mdl-30597394