CareLit · DOI-Nachweis · Klinische Pädiatrie
Intracerebral mass bleeding in a term neonate: Manifestation of hereditary Protein S deficiency with a new mutation in the PROS1 Gene
DOI 10.1055/s-0030-1261588
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Nachweis in CareLit
Autor:innenD Fischer, S Salamat, H Buxmann, A Allendorf, RL Schloesser
ZeitschriftKlinische Pädiatrie
Ausgabe06/2010
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Background: Vitamin K deficiency, birth asphyxia, birth trauma and malformation of blood vessels are the major causes for intracranial bleeding in term neonates and are therefore considered first line in any term neonate with severe haemorrhage. In contrast, the most common manifestation of hereditary prothrombotic disorders during the neonatal period is thrombosis of A. cerebri media or sinus thrombosis. However, t…
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Zitierempfehlung
D Fischer, S Salamat, H Buxmann, A Allendorf, RL Schloesser (2010) Intracerebral mass bleeding in a term neonate: Manifestation of hereditary Protein S deficiency with a new mutation in the PROS1 Gene. Klinische Pädiatrie (06). https://doi.org/10.1055/s-0030-1261588
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