Anemia at the Extremes of Life: Congenital Hemolytic Anemia

2018 ◽  
pp. 95-135
Author(s):  
Ariel L. Reinish ◽  
Suzie A. Noronha
Keyword(s):  
Hemolytic Anemia ◽  
Congenital Hemolytic Anemia

A Case of Congenital Hemolytic Anemia of Unknown Cause Combined with Gilbert's Syndrome

2008 ◽  
Vol 43 (1) ◽  
pp. 58 ◽  
Author(s):  
Ji Whan Lim ◽  
Joon Hyouk Choi ◽  
Yang Hoon Nam ◽  
In Seok Seo ◽  
Seong Min Yoon ◽  
...  
Keyword(s):  
Hemolytic Anemia ◽  
Gilbert’S Syndrome ◽  
Gilbert's Syndrome ◽  
Congenital Hemolytic Anemia

Congenital Hemolytic Anemia with High Sodium, Low Potassium Red Cells

1968 ◽  
Vol 278 (11) ◽  
pp. 573-581 ◽  
Author(s):  
Harold S. Zarkowsky ◽  
Frank A. Oski ◽  
Ramadan Sha'afi ◽  
Stephen B. Shohet ◽  
David G. Nathan
Keyword(s):  
Hemolytic Anemia ◽  
Red Cells ◽  
High Sodium ◽  
Low Potassium ◽  
Congenital Hemolytic Anemia

Clinical and hematologic outcomes after splenectomy for congenital hemolytic anemia

2021 ◽  
Vol 6 (1) ◽  
pp. 41
Author(s):  
RaniaR El Nahal ◽  
MostafaM Embaby ◽  
MotazA El Tayeb ◽  
MohammedH Ghazaly
Keyword(s):  
Hemolytic Anemia ◽  
Congenital Hemolytic Anemia

scholarly journals Severe congenital hemolytic anemia caused by a novel compound heterozygous PKLR gene mutation in a Chinese boy

2019 ◽  
Vol 132 (1) ◽  
pp. 92-95 ◽  
Author(s):  
Peng-Peng Liu ◽  
Hu-Qing Ding ◽  
Shen-Zhen Huang ◽  
Sheng-Yong Yang ◽  
Ting Liu
Keyword(s):  
Gene Mutation ◽  
Hemolytic Anemia ◽  
Compound Heterozygous ◽  
Congenital Hemolytic Anemia

scholarly journals Exome sequencing for diagnosis of congenital hemolytic anemia

2020 ◽  
Vol 15 (1) ◽  
Author(s):  
Lamisse Mansour-Hendili ◽  
Abdelrazak Aissat ◽  
Bouchra Badaoui ◽  
Mehdi Sakka ◽  
Christine Gameiro ◽  
...  
Keyword(s):  
Exome Sequencing ◽  
Hemolytic Anemia ◽  
Congenital Hemolytic Anemia

Congenital Hemolytic Anemia in the Negro

1950 ◽  
Vol 4 (1) ◽  
pp. 1-4
Author(s):  
Lee Ehrlich ◽  
Steven O. Schwartz
Keyword(s):  
Hemolytic Anemia ◽  
Congenital Hemolytic Anemia

scholarly journals Congenital Hemolytic Anemia with Abnormal Pigment Metabolism and Red Cell Inclusion Bodies: a New Clinical Syndrome

Blood ◽  
1958 ◽  
Vol 13 (10) ◽  
pp. 950-958 ◽  
Author(s):  
ROBERT D. LANGE ◽  
JOSEPH H. AKEROYD
Keyword(s):  
Case Report ◽  
Hemolytic Anemia ◽  
Inborn Error ◽  
Inclusion Bodies ◽  
Clinical Syndrome ◽  
Red Cell ◽  
Dark Urine ◽  
Special Studies ◽  
Congenital Hemolytic Anemia

Abstract 1. A case report and special studies of a 14-year-old girl with a congenital hemolytic anemia are reported. 2. Fourteen per cent of her erythrocytes contained unusual inclusion bodies. 3. In addition, the child has been known to pass dark urine since the age of 2½ years. The pigment probably belongs to the bilifuscin and mesobilifuscin group. 4. It is believed that the syndrome is probably caused by an inborn error in erythrocytic metabolism. 5. It has been proposed that the syndrome be named "congenital hemolytic anemia with abnormal pigment metabolism and red cell inclusion bodies."

Pyruvate kinase ?G�ttingen1,2?: Congenital hemolytic anemia, evidence of double heterozygosity, and lack of enzyme cooperativity

1982 ◽  
Vol 60 (4) ◽  
pp. 381-386 ◽  
Author(s):  
W. Schr�ter ◽  
M. Lakomek ◽  
M. Scharnetzky ◽  
W. Tillmann ◽  
H. Winkler
Keyword(s):  
Pyruvate Kinase ◽  
Hemolytic Anemia ◽  
Double Heterozygosity ◽  
Congenital Hemolytic Anemia
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