Factor 10 Deficiency: A Case Report

^1,2Pediatric Resident, ibn Rochd Hospital Hassan 2 University, Morocco

^3,6-8Pediatric Professor, Ibn Rochd Hospital, Hassan 2 University, Morocco

^4,5Pediatric Assistant Professor, ibn Rochd Hospital, Hassan 2 University, Morocco

*Corresponding author: Dr. Salma Tihamy, Pediatric Resident, ibn Rochd Hospital Hassan 2 University, ibn Toufail street N° 11 Farah 1 Settat, Morocco, Phone: 0682688396, Email: [email protected]

Received Date: December 01, 2024

Published Date: January 02, 2025

Citation: Tihamy S, et al. (2025). Evolution of Pediatric Feeding Disorders. Mathews J Pediatr. 10(1):37.

Copyrights: Tihamy S, et al. © (2025).

ABSTRACT

Factor X deficiency is a rare coagulation disorder characterized by early onset, severity and spontaneous hemorrhagic manifestations. We report the case of a male neonate from a consanguineous marriage admitted with intense pallor following bleeding at the site of a blood sample taken as part of the preoperative work-up for active hydrocephalus due to Dandy Walker malformation. The work-up confirmed the presence of factor X deficiency.

Keywords: Hemorrhagic Syndromes, Intra-Ventricular Hemorrhage, Factor X Deficiency.