Results 11 to 20 of about 151,689 (336)

Case report: Glucose 6-phosphate-isomerase deficiency combine with avascular necrosis of bilateral femoral head

Frontiers in Pediatrics, 2022
BackgroundGlucose 6-phosphate-isomerase deficiency (GPI) is an uncommon autosomal recessive genetic disorder characterized by chronic asphoric hemolytic anemia, jaundice, and hepatospleenomegaly of varying degrees.
Zhenqi Song, Kongjian Wang, Djandan Tadum Arthur, Zhongwen Tang, Feng Xiang, Jie Wen, Sheng Xiao   +6 more
doaj   +1 more source

Value of three hemolysis tests and carboxyhemoglobin in the diagnosis of hemolytic disease of the fetus and newborn

Zhongguo shuxue zazhi, 2023
Objective To investigate the value of three hemolysis tests and carboxyhemoglobin (COHb) level in the diagnosis of hemolytic disease of the fetus and newborn (HDFN).
Fan ZHAO, Zhili SHAO, Xiaohan YOU, Jiancheng JIAO, Lili FAN, Min SUN, Lingzhi MENG, Li MA   +7 more
doaj   +1 more source

Incidence and Risk Factors of Cholestasis in Newborns with Hemolytic Disease-A Case-Control Study. [PDF]

J Clin Med
Drozdowska-Szymczak A, Mazanowska N, Pomianek T, Ludwin A, Krajewski P.   +4 more
europepmc   +3 more sources

Rainbow of colors: Inspissated bile syndrome secondary to hemolytic disease of the newborn and concomitant serum dynamics

SAGE Open Medical Case Reports, 2021
The recent clinical experience with hemolytic disease of the newborn and its post-icteric sequelae is limited among high-income countries because of nearly over four decades of effective prevention care.
Veronica Mugarab Samedi, Mehrieh Rahimi, Kaartigean Kalaniti, Martha Lyon, Sibasis Daspal   +4 more
doaj   +1 more source

Non-immune Hemolysis in Gaucher Disease and Review of the Literature Eliyakim Hershkop, Idan Bergman, Alina Kurolap, Najib Dally, and Hagit Baris Feld

Rambam Maimonides Medical Journal, 2021
Gaucher disease (GD) is an autosomal recessive disease characterized by the buildup of glucocerebrosides in macrophages, resulting in the formation of “Gaucher cells.” These cells predominantly infiltrate the liver, spleen, and bone marrow leading to ...
Eliyakim Hershkop, Idan Bergman, Alina Kurolap, Najib Dally, Hagit Baris Feldman   +4 more
doaj   +1 more source

Oblivious of the yellow world – A newborn's telltale: ABO hemolytic disease of newborn

Global Journal of Transfusion Medicine, 2019
The increased destruction of fetal red cells can be immune (allo- or autoantibodies) or nonimmune (hemoglobinopathies, enzyme defects, and membrane defects) in nature and can cause shortened life span of red cells leading to hemolytic disease of the ...
Daljit Kaur, Poonam Sidana, Gaurav Mandhan, Kamlesh Kanodia   +3 more
doaj   +1 more source

Edematous form of the Hemolytic Disease of the Fetus and Newborn

Медицинский вестник Юга России, 2019
Clinical observation of a premature newborn patient with an edematous form of the Hemolytic Disease is presented. A feature of this case is its relative rarity in view of the favorable outcome of the most severe form of hemolytic disease in an extremely ...
M. G. Pukhtinskaya, V. V. Estrin, Yu. A. Porutchikovа, A. V. Simonovа   +3 more
doaj   +1 more source

FEATURES OF ADAPTATION OF NEWBORNS WHO HAVE HAD INTRAUTERINE BLOOD TRANSFUSIONS

Кубанский научный медицинский вестник, 2018
Aim. To assess the adaptive capacity of newborns who have had intrauterine blood transfusions.Materials and methods. The study included 40 newborns who underwent intrauterine intravascular blood transfusion due to hemolytic disease of the fetus RH-factor.
N. V. BOYKO, G. YU. MODEL, V. I. ALEKHINA   +2 more
doaj   +1 more source

Case series: coronavirus disease 2019 infection as a precipitant of atypical hemolytic uremic syndrome: two case reports

Journal of Medical Case Reports, 2021
Background Atypical hemolytic uremic syndrome is an exceedingly rare thrombotic microangiopathy caused by accelerated activation of the alternative complement pathway.
Christine J. Kurian, Zachary French, Patrick Kukulich, Matthew Lankiewicz, Sushil Ghimire, Omar H. Maarouf, Sanaa Rizk, Ruben Rhoades   +7 more
doaj   +1 more source

Acute Tubular Necrosis Associated with Autoimmune Hemolytic Anemia due to Acute Gastroenteritis

Turkish Journal of Internal Medicine, 2021
Autoimmune hemolytic anemia (AIHA) is a rare disease with a rate of 1-3 in 100,000 in adults. AIHA are defined as primary (idiopathic) or secondary depending on the presence or absence of accompanying disease.
Mehmet Sezen, Abdülmecit Yıldız, Mahmut Yavuz, Kamil Dilek, Mustafa Güllülü, Ayşegül Oruç, Mehmet Fethullah Aydın, Alparslan Ersoy   +7 more
doaj   +1 more source