Results 41 to 50 of about 18,745 (222)

Severe hereditary spherocytosis presenting with non-immune fetal hydrops

Indian Pediatrics Case Reports, 2023
Background: Hereditary spherocytosis (HS) is characterized by spherocytes on the peripheral smear and heterogeneous clinical presentation (mild, moderate, moderate/severe, and severe) depending upon the severity of hemolytic anemia, jaundice, and ...
Snehal Mallakmir, Rashid Merchant, Nandkishor S Kabra, Javed Ahmed   +3 more
doaj   +1 more source

Zika virus: New clinical syndromes and its emergence in the western hemisphere [PDF]

, 2016
Zika virus (ZIKV) had remained a relatively obscure flavivirus until a recent series of outbreaks accompanied by unexpectedly severe clinical complications brought this virus into the spotlight as causing an infection of global public health concern.
Brazilian Medical Genetics Society–Zika Embryopathy Task Force, Centers for Disease Control and Prevention, Centers for Disease Control and Prevention, Centers for Disease Control and Prevention, Collaborative Cross Consortium, European Centre for Disease Prevention and Control, European Centre for Disease Prevention and Control, Helen M. Lazear, Michael S. Diamond, T. C. Pierson   +9 more
core   +3 more sources

Twin Anemia Polycythemia Sequence: Knowledge and Insights After 15 Years of Research

Maternal-Fetal Medicine, 2021
. Twin anemia polycythemia sequence (TAPS) is a chronic form of unbalanced feto-fetal transfusion through minuscule placental anastomoses in monochorionic twin pregnancies, leading to anemia in the donor twin and polycythemia in the recipient twin.
Lisanne S.A. Tollenaar, Enrico Lopriore, Dick Oepkes, Monique C. Haak, Frans J.C.M. Klumper, Johanna M. Middeldorp, Jeanine M.M. Van Klink, Femke Slaghekke, Yang Pan   +8 more
doaj   +1 more source

Quality control in blood irradiation

Brazilian Journal of Radiation Sciences, 2023
Irradiation is a technique used in hemotherapy to functionally inactivateviable lymphocytes, in cellular blood components, to reduce the risk of Transfusion-associated Graft-versus-Host Disease (AT-GVHD), is rare but letal.
F. Lopes, R.C.G. Rocha, E. Munhoz, F.C. Trigo, V.B.E.R. Feijó, M. Fernandes, T.C. De Paula, L.G. Padilha Filho, G.S. Araujo   +8 more
doaj   +1 more source

Chelation therapy for secondary neonatal iron over load: Lessons learned from rhesus hemolytic disease

The Turkish Journal of Pediatrics, 2018
Secondary neonatal iron overload occurs with intrauterine and post-natal blood transfusions. Treatment with intravenous Deferoxamine was reported only in four cases in the literature.
Fareed Khdair-Ahmad, Tariq Aladily, Olfat Khdair-Ahmad, Eman F Badran   +3 more
doaj   +1 more source

Intraperitoneal and intracardiac transfusion of recurrent fetal erythroblastosis due to anti-M alloimmunization with unfavorable outcome

Taiwanese Journal of Obstetrics & Gynecology, 2012
Objective: To present intensive intrauterine treatment of recurrent early onset fetal erythroblastosis due to anti-M alloimmunization. Case Report: A 33-year-old woman, gravid 3, para 1, had anti-M IgG antibody, which caused alloimmunization of her ...
Tzu-Hung Lin, Jin-Chung Shih, Chia-Hui Lin, Shin-Yu Lin, Yi-Ning Su, Chien-Nan Lee   +5 more
doaj   +1 more source

Doppler middle cerebral artery peak systolic velocity measurement as diagnostic tool for fetal anemia after in-utero transfusions in red blood cell alloimmunisation [PDF]

Vojnosanitetski Pregled, 2020
Background/Aim. Doppler sonography of fetal middle cerebral artery peak systolic velocity (MCA-PSV) can be used to predict fetal anemia and the need for in utero intravascular transfusion (IUIT) in red blood cell (RBC) alloimmunisation pregnancies.
Marjanović-Cvjetićanin Mirjana, Plešinac Snežana, Dotlić Jelena, Plećaš Darko, Kocijančić-Belović Dušica, Akšam Slavica   +5 more
doaj   +1 more source

Iron Deficiency Anemia: An Unexpected Cause of an Acute Occipital Lobe Stroke in an Otherwise Healthy Young Woman [PDF]

, 2020
A 29-year-old caucasian woman who presented to the hospital with an acute onset of right eye visual disturbance and headache was found to have an acute left occipital lobe infarction.
Nace, Travis C, O\u27Sullivan, Conor, Shan, Khine S, Zhang, Qian   +3 more
core   +1 more source

Retrieval and Registration of Long-Range Overlapping Frames for Scalable Mosaicking of In Vivo Fetoscopy [PDF]

, 2018
Purpose: The standard clinical treatment of Twin-to-Twin Transfusion Syndrome consists in the photo-coagulation of undesired anastomoses located on the placenta which are responsible to a blood transfer between the two twins.
Attilakos, George, Deprest, Jan, Ourselin, Sébastien, Peter, Loïc, Shakir, Dzhoshkun Ismail, Tella-Amo, Marcel, Vercauteren, Tom, Wimalasundera, Ruwan   +7 more
core   +2 more sources

Genotype–Phenotype Correlation in TTC7A‐Associated Gastrointestinal Defects and Immunodeficiency Syndrome 1

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Gastrointestinal defects and immunodeficiency syndrome 1 (GIDID1) is a rare autosomal recessive disorder caused by biallelic variants in TTC7A. GIDID1 is characterized by a broad clinical spectrum ranging from very early‐onset inflammatory bowel disease (VEOIBD) to multiple intestinal atresia (MIA) with or without immunological manifestations.
Julia Imhoff, Hans Christian Schmidt, Matthias Hans Belau, Johanna Hagens, Mario Lange, Daniel Tegtmeyer, Konrad Reinshagen, Frederike Leonie Harms, Christian Tomuschat   +8 more
wiley   +1 more source