Results 101 to 110 of about 10,139 (212)

Fatal course of ABO hemolytic disease associated with hydrops in a twin pregnancy

The Turkish Journal of Pediatrics, 2006
Hydrops fetalis associated with ABO incompatibility is an extremely rare condition. We report twin infants both afflicted with significant ABO hemolytic disease but showing different degrees of clinical severity, in which fatal hydrops developed ...
Filiz Tiker, Berkan Gürakan, Aylin Tarcan, Namik Ozbek   +3 more
doaj  

Hydrops fetalis

Archives of Cardiovascular Imaging, 2014
Kriengkrai Iemsawatdikul, Heike E. Daldrup-Link   +1 more
  +6 more sources

437: Underlying etiologies in prenatally-diagnosed non-immune hydrops fetalis [PDF]

, 2018
Datkhaeva, Ilina, Fratto, Victoria, Laurent, Louise, Lianoglou, Billie, Mardy, Anne H, Murphy, Aisling M, Norton, Mary E, Sparks, Teresa N, Thao, Kao, Wilson, Lisa   +9 more
core   +1 more source

Early onset Mirror Syndrome associated with foetal sacrococcigeal teratoma: a rare entity [PDF]

, 2013
In the mirror syndrome, maternal symptoms mime foetal and placental oedema. The pathogenesis is unknown. The most common etiologic associations are rhesus isoimmunization, twin-twin transfusion syndrome and viral infections.
ALIMONDI, Pietro, Calagna, Gloria, CUCINELLA, Gaspare, LO DICO, Giuseppe, MARESI, Emiliano, ORLANDI, Emanuela, PERINO, Antonino, RINOLDO, Calogero, TIBERIO, Francesca, VENEZIA, Renato   +9 more
core  

Identification of α°-thalassaemia (–SEA) using an enzyme-linked immunosorbent assay (ELISA) for embryonic zeta-globin chain detection – a preliminary study [PDF]

, 2006
Objectives: This study aimed to evaluate the UBI MAGIWELTM ζ-GLOBIN ELISA Kit for the presumptive diagnosis of αo-thalassaemia. The ELISA results obtained were confirmed by molecular characterisation of αo-thalassaemia using a Duplex-PCR.
George, Elizabeth, Hassan, R., Lim, E. J., Tan, K. L., Tan, Mary Anne Jin Ai, Wee, Y. C., Zakaria, Z.   +6 more
core  

Congenital tuberculosis causing hydrops fetalis: A case report and review of literature. [PDF]

J Family Med Prim Care, 2023
Bansal E, Mehra S, Bhalla K.
europepmc   +1 more source

Penatalaksaan Pada Pasien Talasemia [PDF]

, 2013
Latar Belakang. Talasemia adalah sekelompok anemia hipokromik mikrositer herediter dengan berbagai derajat keparahan. Di seluruh dunia, 15 juta orang memiliki presentasi klinis dari talasemia.
Yunitha, R. A. (Rini)
core  

Immunglobuline, materno-fetaler Transport, fatale Folgen [PDF]

, 1993
Brusis, E.
core   +1 more source

Detection on common deletional alpha thalassaemia in pregnant women by polymerase chain reaction techniques [PDF]

, 2015
Thalassaemia is the most common inherited disorder worldwide and represent as a major health problem in many areas and approximately 4.5%- 6% of Malaysians are carrier of this genetic disorder.
Fathma Abdullah, Nurul Ain
core  

Parvovirus: Conservative management of fetal anemia and hydrops

Acta Obstetricia et Gynecologica Scandinavica
Following the COVID‐19 pandemic, Northwestern Europe has experienced a marked increase in congenital parvovirus infections. This rise is attributed to social distancing measures which disrupted the usual seasonal variation of parvovirus B19.
Lyndsay Creswell, Pranav Pandya, Daniel Stott, Donald Peebles, George Attilakos, Eleni Nastouli, Haley Alchin, Kelly Pegoretti Baruteau, Raffaele Napolitano   +8 more
doaj   +1 more source