Coagulation factor XIII deficiency - Report of a newborn F13A1 Val34Leu polymorphism carrier
Coagulation factor XIII deficiency (FXIIID) is a rare inherited autosomal recessive bleeding disorder. FXIIID is the only coagulation factor deficiency that has been associated with pregnancy loss. Regarding neonates, prolonged umbilical cord bleeding and intracranial hemorrhage, a life-threatening...
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| Main Authors: | , , , , |
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| Format: | Book |
| Published: |
Hygeia Press di Corridori Marinella,
2022-10-01T00:00:00Z.
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Internet
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |