Recurrent intraparenchymal brain hemorrhage in an infant with factor XIII deficiency
Factor XIII deficiency is an autosomal recessive disorder with an incidence of 1 in 1-5 million. On activation factor XIII stabilizes clot formation by cross-linking fibrin strands. Deficiency is characterized by severe bleeding due to impairment in clot formation. We describe a case of a child pres...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Hygeia Press di Corridori Marinella,
2021-05-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |