Hb C disease

Networked: 8 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Hemic and Lymphatic Diseases: 6
- Hematologic Diseases: 3366
  - Anemia: 38331
    - Hemolytic Anemia: 6695
      - Congenital Hemolytic Anemia: 288
        Hemoglobin C Disease: 21
        Hb C disease: 8
  - Hemoglobinopathies: 2001
    - Hemoglobin C Disease: 21
      - Hb C disease: 8
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Hemoglobinopathies: 2001
    - Hemoglobin C Disease: 21
      - Hb C disease: 8
  - Congenital Hemolytic Anemia: 288
    - Hemoglobin C Disease: 21
      - Hb C disease: 8

Related Diseases

1.	Sickle Cell Anemia (Hemoglobin S Disease)
2.	Hemoglobin SC Disease (Disease, Hemoglobin SC)
3.	Thalassemia
4.	Sickle Cell Trait

Experts

1.	DiNello, Robert K: 1 article (11/2016)
2.	Geisberg, Mark: 1 article (11/2016)
3.	Panchal, Anand: 1 article (11/2016)
4.	Paniagua, Mary C: 1 article (11/2016)
5.	Quinn, Charles T: 1 article (11/2016)
6.	Agosti, Steven J: 1 article (01/2007)
7.	Man, Mary A: 1 article (01/2007)
8.	Mastorides, Stephen M: 1 article (01/2007)
9.	Thomas, L Brannon: 1 article (01/2007)
10.	Hagar, Arthur F: 1 article (02/2004)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Hb C disease:

1.	Hemoglobins (Hemoglobin)IBA 03/03/1975 - "The other patient, with sickle cell hemoglobin Hb A, S, and (Hb) C disease, also achieved an 80% exchange calculated on the level of HbA.S. " 09/01/1998 - "The clinical and biological heterogeneity of sickle cell hemoglobin (Hb) C disease (SC disease) is similar to sickle cell anemia, but has a much milder course. " 04/01/1972 - "Chemical heterogeneity of fetal hemoglobin in subjects with sickle cell anemia, homozygous Hb-C disease, SC disease, and various combinations of hemoglobin variants."
2.	Fetal Hemoglobin (Hemoglobin F)IBA 04/01/1972 - "Chemical heterogeneity of fetal hemoglobin in subjects with sickle cell anemia, homozygous Hb-C disease, SC disease, and various combinations of hemoglobin variants."
3.	Hydromorphone (Dilaudid)FDA LinkGeneric 06/01/2023 - "Those 18 years or older admitted with one of the following International Classification of Diseases, Tenth Revision codes were included: D57.0 (Hb-SS disease with crisis), D57.2 (sickle cell/Hb-C disease), and D57.4 (sickle cell thalassemia), and administered PCA or IVP hydromorphone. "
4.	AlkaliesIBA 08/01/1985 - "In both cases of homozygous Hb C disease and Hb SC disease the Hb F level by alkali denaturation was less than 1% and the microchromatographic Hb F level was 0.7%. "
5.	hemoglobin RaleighIBA 01/01/2007 - "In 252 cases, sickle cell trait was identified with a mean retention time (RT) of 1.44 (SD +/-0.02) min. In 82 cases, Hb C trait was identified with a mean RT of 1.66 +/-0.03 min. RTs for other Hb abnormalities, including sickle cell disease, homozygous Hb C disease, C Harlem trait, alpha-chain Hb variants, Hb D trait, Hb G trait, Hb J trait, Hb Raleigh, and Hb Lepore were also determined. "
6.	hemoglobin Iowa (Hb Iowa)IBA 02/01/2004 - "We conclude that the presence of Hb Iowa, or other variants with similar pIs, should be considered in cases where the results of follow-up testing conflict with neonatal diagnosis of sickle cell or Hb C disease, or where clinical presentation does not agree with diagnosis of either homozygous or heterozygous Hb S or Hb C." 02/01/2004 - "Neonatal misidentification of Hb Iowa led to misdiagnosis of sickle cell disease and Hb C disease, respectively. "
7.	hemoglobin LeporeIBA 01/01/2007 - "In 252 cases, sickle cell trait was identified with a mean retention time (RT) of 1.44 (SD +/-0.02) min. In 82 cases, Hb C trait was identified with a mean RT of 1.66 +/-0.03 min. RTs for other Hb abnormalities, including sickle cell disease, homozygous Hb C disease, C Harlem trait, alpha-chain Hb variants, Hb D trait, Hb G trait, Hb J trait, Hb Raleigh, and Hb Lepore were also determined. "
8.	hemoglobin DIBA 01/01/2007 - "In 252 cases, sickle cell trait was identified with a mean retention time (RT) of 1.44 (SD +/-0.02) min. In 82 cases, Hb C trait was identified with a mean RT of 1.66 +/-0.03 min. RTs for other Hb abnormalities, including sickle cell disease, homozygous Hb C disease, C Harlem trait, alpha-chain Hb variants, Hb D trait, Hb G trait, Hb J trait, Hb Raleigh, and Hb Lepore were also determined. "
9.	hemoglobin ASIBA 11/01/2016 - "The accuracy of HemoTypeSC™ was evaluated on 100 whole blood samples from individuals with common relevant haemoglobin phenotypes, including normal (Hb AA, N = 20), carrier or trait (Hb AS, N = 22; Hb AC, N = 20), SCD (Hb SS, N = 22; Hb SC, N = 13), and Hb C disease (Hb CC, N = 3). "