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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Phenotype and genotype of FXIII deficiency in two unrelated probands: identification of a novel F13A1 large deletion mediated by complex rearrangement

Fig. 1

Fetal bleedings and delayed wound healings in probands 1 and 2. a and b Cerebral hemorrhage of the left top occipital lobe at the beginning and 17 days later, respectively shown by computed tomography (CT) in proband 1, indicated by the arrows; c and d Spinal cord hematoma located at T12-L2 at the time of diagnosis and 4 days later, respectively, revealed by magnetic resonance imaging (MRI) in proband 2, indicated by the arrows; e-h Four wounds resulting from delayed wound healing in proband 2. e Forehead; f Right hip; g Left abdomen; h Right thigh

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172