|
Total: 32 |
|
| PMID (PMCID) | ||
|---|---|---|
|
31110746 |
OTHER | |
| Particular etiology in a case of peripheral tetraparesis. | ||
|
Gheorghe GS, Hodorogea AS, Gheorghe ACD, Zaharia OIR, Neacsu O, Nanea IT, Ciobanu A. Clin Case Rep. 2019;7(5):1062-1066. |
||
| We report the case of nonprofessional lead intoxication manifested by tetraparesis, severe anemia, and hemolysis in a patient having also unknown beta thalassemia minor. | ||
|
28428899 (5385913) |
OTHER | |
| Watershed Infarct in Beta-Thalassemia Major Patient. | ||
|
Ansari B, Saadatnia M, Asghar Okhovat A. Case Rep Neurol Med. 2017;2017:2736402. |
||
| However, there is no report of watershed infarct in beta-thalassemia anemia. | ||
|
25000650 |
FEMALE | Adult |
| Notorious anti-Jk3 in a pregnant woman. | ||
|
Jator EK. Clin Lab Sci. 2014;27(2):78-82. |
||
| This patient, with a history of mild anemia due to beta-thalassemia minor and two known transfusion of packed red cells came to an emergency room complaining of severe abdominal cramps. | ||
|
22766185 |
FEMALE | Adult |
| [Unusual aspect of pernicious anemia during association of beta-thalassemia: a new case report and literature review]. | ||
|
Diop MM, Toure PS, Leye MY, Leye A, El Fadjri S, Diop M, Ka MM, Diop OD, Fall S, Ndiaye FS. Mali Med. 2012;27(1):71-2. |
||
| [Unusual aspect of pernicious anemia during association of beta-thalassemia: a new case report and literature review]. | ||
|
19788508 |
FEMALE | Infant |
| Delayed hemolytic transfusion reaction with hyperhemolysis after first red blood cell transfusion in child with beta-thalassemia: challenges in treatment. | ||
|
Hannema SE, Brand A, van Meurs A, Smiers FJ. Transfusion. 2010;50(2):429-32. |
||
| A 1.5-year-old girl with homozygous beta-thalassemia was put on a regular RBC transfusion program because of anemia with stunted growth and abnormal bone development. | ||
|
20594021 |
MALE | Middle Aged |
| Extramedullary hematopoietic tumor mimicking a thoracic nerve root schwannoma. | ||
|
Oermann EK, Coppa ND, Margolis M, Sandhu FA. J Neurosurg Spine. 2010;13(1):78-81. |
||
| The authors report the case of a 51-year-old man with beta-thalassemia and chronic anemia who was found to have a 4-cm paravertebral mass suggestive of a schwannoma. | ||
|
20353356 |
MIXED_SAMPLE | Infant |
| Molecular characterization of a Chinese pedigree with beta-thalassemia intermedia. | ||
|
Huang G, Jiang WL, Rong KB, Li YX, Luo XL, Meng JX, Yu XY. Hemoglobin. 2010;34(2):179-83. |
||
| Hereditary persistence of fetal hemoglobin (HPFH), often associated with mutations in the beta-globin gene cluster, is normally benign, but a person carrying both HPFH and another beta-thalassemia (beta-thal) mutation will develop serious anemia. | ||
|
19624489 |
MALE | Young Adult |
| Alloanti-c/ce in a c+ceAR/Ce patient suggests that the rare RHCE ceAR allele (ceAR) encodes a partial c antigen. | ||
|
Peyrard T, Pham BN, Poupel S, Martin-Blanc S, Auxerre C, Kappler-Gratias S, Bonin P, Rouger P, Le Pennec PY. Transfusion. 2009;49(11):2406-11. |
||
| A 21-year-old patient suffering from intermediate beta-thalassemia, with transfusion history, was hospitalized for severe anemia. | ||
|
19034506 |
FEMALE | Infant |
| Interaction of Hb South Florida (codon 1; GTG-->ATG) and HbE, with beta-thalassemia (IVS1-1; G-->A): expression of different clinical phenotypes. | ||
|
Tan JA, Tan KL, Omar KZ, Chan LL, Wee YC, George E. Eur J Pediatr. 2009;168(9):1049-54. |
||
| HbE-beta-thalassemia generally manifests with severe anemia where individuals exhibit beta-thalassemia major with regular blood transfusions or beta-thalassemia intermedia with periodic blood transfusions. | ||
|
19536514 |
MALE | Adult |
| [Severe microcytic anemia with megaloblastic changes in the bone marrow. A hematological paradoxon?]. | ||
|
Reibke R, Hausmann A, Cnossen J, Hiddemann W, Spiekermann K, Braess J. Internist (Berl). 2009;50(7):881-6. |
||
| The paradoxon therefore dissolved as a pernicious anemia with megaloblastic changes with microcytic erythrocytes due to beta-thalassemia. | ||
|
19536514 |
MALE | Adult |
| [Severe microcytic anemia with megaloblastic changes in the bone marrow. A hematological paradoxon?]. | ||
|
Reibke R, Hausmann A, Cnossen J, Hiddemann W, Spiekermann K, Braess J. Internist (Berl). 2009;50(7):881-6. |
||
| Further work-up verified beta-thalassemia minor and revealed severely decreased vitamin B12 levels with positive anti intrinsic-factor antibodies, pathognomonic for autoimmune pernicious anemia. | ||
|
18246369 |
FEMALE | |
| Crohn's disease, autoimmune thyroiditis, and beta-thalassemia trait in an adolescent: an unusual combination of diseases. | ||
|
Bank I, Busari JO. Eur J Pediatr. 2008;167(11):1343-6. |
||
| Clinical and laboratory evaluation revealed a microcytemic anemia with iron deficiency, beta thalassemia, and thyrotoxicosis with thyroid antibodies. | ||
|
17805044 |
MALE | |
| An Iranian child with HbQ-Iran [alpha75 (EF4) Asp-->His]/-alpha3.7 kb/IVSII.1 G-->A: first report. | ||
|
Rahimi Z, Akramipour R, Vaisi-Raygani A, Nagel RL, Muniz A. J Pediatr Hematol Oncol. 2007;29(9):649-51. |
||
| This report indicates that HbQ-Iran to be a benign structural variant of Hb, that in combination with -alpha3.7 kb gene and beta0-thalassemia, presents a minor beta-thalassemia picture with moderate anemia. | ||
|
15755051 |
FEMALE | Adult |
| Erythropoietin use in a pregnant Jehovah's witness with anemia and beta-thalassemia: a case report. | ||
|
Bennett M, Macri CJ, Bathgate SL. J Reprod Med. 2005;50(2):135-7. |
||
| A 26-year-old, African American woman belonging to the Jehovah's Witness sect presented with anemia associated with beta-thalassemia. | ||
|
15755051 |
FEMALE | Adult |
| Erythropoietin use in a pregnant Jehovah's witness with anemia and beta-thalassemia: a case report. | ||
|
Bennett M, Macri CJ, Bathgate SL. J Reprod Med. 2005;50(2):135-7. |
||
| We treated anemia caused by beta-thalassemia in pregnancy with synthetic erythropoietin to avoid a transfusion in a Jehovah's Witness. | ||
|
15755051 |
FEMALE | Adult |
| Erythropoietin use in a pregnant Jehovah's witness with anemia and beta-thalassemia: a case report. | ||
|
Bennett M, Macri CJ, Bathgate SL. J Reprod Med. 2005;50(2):135-7. |
||
| Erythropoietin use in a pregnant Jehovah's witness with anemia and beta-thalassemia: a case report. | ||
|
12187108 |
MALE | Adult |
| Renal tubular dysfunction in a patient with beta-thalassemia minor. | ||
|
Oktenli C, Bulucu F. Nephron. 2002;92(1):222-3. |
||
| Based upon the detailed evaluation for both asymptomatic urinary abnormality and anemia, he was diagnosed as having renal tubular dysfunction and beta-thalassemia minor (hemoglobin A(1)was 91%, and hemoglobin A(2)was 9%). | ||
|
10532663 |
MIXED_SAMPLE | Child |
| Tubulointerstitial renal failure in childhood leptospirosis. | ||
|
Vachvanichsanong P, Dissaneewate P, Mitarnun W. Pediatr Emerg Care. 1999;15(5):332-4. |
||
| Only one child, who had an underlying disease of beta-thalassemia/Hb E, had jaundice, hepatosplenomegaly, anemia, and thrombocytopenia. | ||
|
8037185 |
MIXED_SAMPLE | Infant |
| Beta-thalassemia alleles and unstable hemoglobin types among Russian pediatric patients. | ||
|
Curuk MA, Molchanova TP, Postnikov YuV , Pobedimskaya DD, Liang R, Baysal E, Kolodey S, Smetanina NS, Tokarev YuN , Rumyantsev AG, et al.. Am J Hematol. 1994;46(4):329-32. |
||
| This condition and two new variants have the characteristics of a dominant type of beta-thalassemia heterozygosity with moderate anemia, Heinz body formation, splenomegaly, etc. | ||
|
7825242 |
FEMALE | |
| Plasma exchange in refractory autoimmune anemia in a child with systemic vasculitis associated with homozygote beta thalassemia. | ||
|
Besbas N, Ozen S, Bakkaloglu A, Gurgey A, Kanra T, Saatci U. Turk J Pediatr. 1994;36(4):337-40. |
||
| Plasma exchange in refractory autoimmune anemia in a child with systemic vasculitis associated with homozygote beta thalassemia. | ||