We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.
To save content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about saving content to .
To save content items to your Kindle, first ensure no-reply@cambridge.org
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
This chapter focuses on fetal and neonatal alloimmune thrombocytopenia (FNAIT), which is one of the major causes of both severe thrombocytopenia and intracranial hemorrhage (ICH) in fetuses and term neonates. FNAIT is caused by maternal immunization against human platelet antigens (HPAs) on fetal platelets, inherited from the father and different from those present in the mother. The chapter also focuses on the current insights in the etiology, diagnosis, and management of pregnancies at known risk of FNAIT. The diagnosis of FNAIT is unequivocal when paternal incompatibility with corresponding maternal alloantibodies is present. The primary goal of the management of a neonate with FNAIT is to prevent or stop thrombocytopenic bleeding. In suspected cases of FNAIT, babies with severe thrombocytopenia can be transfused with random platelets transfusions, until the diagnosis is established and matched platelets are available.
Recommend this
Email your librarian or administrator to recommend adding this to your organisation's collection.