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Deficiencia congénita grave del factor X como primer caso reportado en Camboya
Chin Soey1, Meang Sovandos1, Lam Pechkethia1
1Department of Pediatric Hematology and Immunology, National Pediatric Hospital, Phnom Penh, Cambodia.
Case reports in hematology
|September 2, 2025
Resumen
Un niño camboyano con síntomas graves fue diagnosticado con deficiencia de factor X, un raro trastorno hemorrágico. El plasma fresco congelado manejó eficazmente su sangrado, destacando su importancia en áreas con recursos limitados.
Área de la Ciencia:
- Hematología
- La genética
- Pediatría
Sus antecedentes:
- La deficiencia del factor X (FX) es un trastorno hereditario autosómico recesivo de baja prevalencia.
- Anteriormente no se habían notificado casos de deficiencia de divisas en Camboya.
- La consanguinidad aumenta el riesgo de enfermedades genéticas raras.
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