Results 31 to 40 of about 2,260 (197)

Acute fetal anemia diagnosed by middle cerebral artery Doppler velocimetry in stage v twin-twin transfusion syndrome. [PDF]

open access: yes, 2011
In stage V twin-twin transfusion syndrome (TTTS), up to 50% of surviving twins die or experience permanent disabilities, likely due to acute intertwin hemorrhage resulting in sudden severe anemia of the survivor.
Friedrich, Esther   +3 more
core   +2 more sources

A very preterm infant born to mother of mirror syndrome secondary to fetomaternal hemorrhage: a case report

open access: yesBMC Pregnancy and Childbirth, 2021
Background Mirror syndrome (MS) is defined as maternal edema with fetal hydrops and placental edema with different etiologies, such as rhesus isoimmunization and twin-twin transfusion syndrome.
Sijie Song   +9 more
doaj   +1 more source

Hydrops Fetalis and Mirror Syndrome Secondary to Rh-D Alloimmunization, Associated with Oligohydramnious: A Case Report

open access: yesCase Reports in Clinical Practice, 2022
One of the most common causes of fetal anemia is red cell alloimmunization. The most common routes of maternal sensitization are via blood transfusion or fetomaternal hemorrhage.
Fatemeh Rahimi-Sharbaf   +3 more
doaj   +1 more source

Placental haemangioma associated with acute fetal anemia in labour.

open access: yesActa Médica Portuguesa, 1990
A case of pregnancy complicated by a placental hemangioma is presented. This was unassociated with any of the complications commonly coexistant with this tumor, and presented with fetal anemia due to a fetomaternal transfusion.
A M Franca-Martins   +3 more
doaj   +1 more source

Prevalence of gestational thrombocytopenia and its effect on maternal and fetal outcome

open access: yesIraqi Journal of Hematology, 2019
BACKGROUND: Gestational thrombocytopenia (GT) is considered as the most common cause of thrombocytopenia in pregnancy and accounts for about 75% of cases.
Vijay Zutshi   +3 more
doaj   +1 more source

Severe intracranial haemorrhage in neonatal alloimmune thrombocytopenia [PDF]

open access: yes, 2011
Neonatal alloimmune thrombocytopenia is a rare (1/1000-5000 births) life-threatening disorder, caused by fetomaternal incompatibility for a fetal human platelet alloantigen inherited from the father, with production of maternal alloantibodies against ...
Morais, S   +5 more
core   +1 more source

Classification of stillbirths is an ongoing dilemma [PDF]

open access: yes, 2016
Aim: To compare different classification systems in a cohort of stillbirths undergoing a comprehensive workup; to establish whether a particular classification system is most suitable and useful in determining cause of death, purporting the lowest ...
Bonaccorsi, Gloria   +9 more
core   +1 more source

A prospective study on the prevalence of red cell alloimmunization via fetomaternal hemorrhage and its association with bad obstetric history

open access: yesGlobal Journal of Transfusion Medicine, 2023
Background and Objectives: The presence of irregular red cell antibodies in the serum of pregnant women is named maternal alloimmunization. Sensitizing events such as traumatic delivery and miscarriage can cause fetomaternal hemorrhage, increasing the ...
Divya Vijayakumar   +3 more
doaj   +1 more source

Application of flow cytometry in transfusion medicine: The Sanjay Gandhi Post Graduate Institute of Medical Sciences, India experience

open access: yesAsian Journal of Transfusion Science, 2022
The application of flow cytometry (FC) is diverse and this powerful tool in used in multiple disciplines such as molecular biology, immunology, cancer biology, virology, and infectious disease screening.
Rajendra Chaudhary, Sudipta Sekhar Das
doaj   +1 more source

A rare manifestation of neonatal alloimmune thrombocytopaenia [PDF]

open access: yes, 2014
Neonatal alloimmune thrombocytopaenia (NAIT) results from a fetomaternal incompatibility with maternal sensitisation against a fetal human platelet antigen (HPA) and antibodies transfer to the fetal circulation, leading to platelet destruction.
Azenha, C   +3 more
core   +1 more source

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