Molecular characterization of rare D--/D--variants in individuals of Indian origin
S Kulkarni, G Mishra, H Maru, D Parchure… - Blood …, 2020 - pmc.ncbi.nlm.nih.gov
Background Rh antigens are critical in haemolytic disease of the foetus and newborn
(HDFN). The D--phenotype is a rare blood group characterised by the lack of expression of …
(HDFN). The D--phenotype is a rare blood group characterised by the lack of expression of …
Successful Management of Severe Early-Onset Fetal Hemolytic Anemia Due to Anti-Rh17 Alloimmunization: A Case Report
SN Ghalandarpoor-Attar, F Rahimi-Sharbaf… - Journal of Obstetrics …, 2023 - jogcr.com
As widespread prophylaxis with anti-D Antibodies has dramatically diminished anti-D-
associated hemolytic disease of the newborn (HDN), other antibodies-associated HDN has …
associated hemolytic disease of the newborn (HDN), other antibodies-associated HDN has …
The Molecular Diagnosis and Management of Rare D--/D--Variants within a Family of Iranian Descent
M Setayeshnezhad, A Oodi, MA Jalali Far - Available at SSRN 5034816 - papers.ssrn.com
Abstract Anti-Hr0 (Anti-Rh17) is an uncommon antibody to high-frequency antigens within
the Rh blood group system. It is found in individuals who do not possess the typical antigens …
the Rh blood group system. It is found in individuals who do not possess the typical antigens …
[引用][C] Hemolytic disease of newborn: beyond Rh-D and ABO incompatibility
A Karanam, P Bandiya - Indian Pediatrics, 2021 - Springer
A full term female baby, with a birth weight of 2.24 kg presented with yellowish discoloration
of eyes and skin at 18 hours of life. Antenatally, there was no evidence of fetal anemia or …
of eyes and skin at 18 hours of life. Antenatally, there was no evidence of fetal anemia or …