Hemoglobin D-Punjab: Difference between revisions
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Within the medical specialty of [[hematology]], '''Hemoglobin D-Punjab''' |
Within the medical specialty of [[hematology]], '''Hemoglobin D-Punjab''', also known as '''hemoglobin D-Los Angeles''',<ref name=":0">{{Cite journal |last=Torres |first=Lidiane de Souza |last2=Okumura |first2=Jéssika Viviani |last3=Silva |first3=Danilo Grünig Humberto da |last4=Bonini-Domingos |first4=Claudia Regina |date=March 2015 |title=Hemoglobin D-Punjab: origin, distribution and laboratory diagnosis |url=https://www.scielo.br/j/rbhh/a/9Kb4Kp98MGvDBbQqrHzXqnz/?format=html&lang=en |journal=Revista Brasileira de Hematologia e Hemoterapia |language=en |volume=37 |pages=120–126 |doi=10.1016/j.bjhh.2015.02.007 |issn=1516-8484}}</ref> '''D-North Carolina''', '''D-Portugal''', '''D-Oak Ridge''', and '''D-Chicago'''<ref name=":1">{{Cite journal |last=El-Kalla |first=S. |last2=Mathews |first2=A. R. |date=January 1997 |title=HB D-Punjab in the United Arab Emirates |url=http://dx.doi.org/10.3109/03630269709000669 |journal=Hemoglobin |volume=21 |issue=4 |pages=369–375 |doi=10.3109/03630269709000669 |issn=0363-0269}}</ref>, is a [[Hemoglobin variants|hemoglobin variant]]. It originates from a [[point mutation]] in the [[human β-globin locus]] and is one of the most common hemoglobin variants worldwide.<ref name=":0" /> It is so named because of its higher prevalence in the [[Punjab region]] of [[India]] and [[Pakistan]], along with northern China, and North America. It is also the most frequent hemoglobin variant in [[Xinjiang Uyghur Autonomous Region]] of [[China]], with a 1997 study indicating that Hemoglobin D-Punjab accounts for 55.6% of the total hemoglobin variants.<ref name=":1" /> |
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Hemoglobin D is a result of a mutation in the one or both of the Beta-chains that make up hemoglobin molecules. Having one gene effected is referred to as trait; having two is referred to as homozygous "disease" although the symptoms of this disease are mild. |
Hemoglobin D is a result of a mutation in the one or both of the Beta-chains that make up hemoglobin molecules. Having one gene effected is referred to as trait; having two is referred to as homozygous "disease" although the symptoms of this disease are mild. |
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== History == |
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Hemoglobin D-Punjab was first discovered in the early 1950s in a mixed British and American family of Indian origin from the [[Los Angeles]] area; hence it is also sometimes called “D Los Angeles”. Hemoglobin D is the 4th most common hemoglobin variant. It developed as a response to the selective pressures of malaria in these regions of Asia.{{citation needed|date=December 2013}} |
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Until the early 1950s, [[hemoglobin A]] and some of its variants had been identified, such as [[hemoglobin S]] and [[hemoglobin C]]. Hemoglobin D was discovered in 1951 with one source stating it was the third variant discovered,<ref name=":1" /> and another source claiming it was the fourth.<ref name=":0" /> Later in 1962, it was found that five other regional variants of hemoglobin D all had the same chemical structure termed hemoglobin D-Punjab.<ref name=":0" /> |
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==Hemoglobin D Trait== |
==Hemoglobin D Trait== |
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==Symptoms== |
==Symptoms== |
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usually present with mild hemolytic anemia and mild to moderate splenomegaly. |
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Even homozygous Hemoglobin D disease does not typically cause clinically significant symptoms. Occasionally it can cause mild haemolytic [[anaemia]] and mild [[splenomegaly]]. The anemia usually occurs in the first few months of life, as fetal hemoglobin decreases and hemoglobin D increases.{{citation needed|date=December 2013}} |
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Even homozygous Hemoglobin D disease does not typically cause clinically significant symptoms. It is usually present with mild haemolytic [[anaemia]] and moderate [[splenomegaly]].<ref>{{Cite journal |last=Pandey |first=Sanjay |last2=Mishra |first2=Rahasya Mani |last3=Pandey |first3=Sweta |last4=Shah |first4=Vineet |last5=Saxena |first5=Renu |date=2012 |title=Molecular characterization of hemoglobin D Punjab traits and clinical-hematological profile of the patients |url=https://www.scielo.br/j/spmj/a/h5fx4tCzbgmfmGxGZC8qrtz/ |journal=Sao Paulo Medical Journal |language=en |volume=130 |pages=248–251 |doi=10.1590/S1516-31802012000400008 |issn=1516-3180}}</ref> The anemia usually occurs in the first few months of life, as fetal hemoglobin decreases and hemoglobin D increases.{{citation needed|date=December 2013}} |
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Hb D-Punjab becomes significant when it is co-inherited with Hb S or B thalassemia. |
Hb D-Punjab becomes significant when it is co-inherited with Hb S or B thalassemia. |
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Revision as of 15:30, 8 December 2023
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| Hemoglobin D-Punjab | |
|---|---|
| Other names | Hemoglobin D disease |
| Specialty | Hematology |
Within the medical specialty of hematology, Hemoglobin D-Punjab, also known as hemoglobin D-Los Angeles,[1] D-North Carolina, D-Portugal, D-Oak Ridge, and D-Chicago[2], is a hemoglobin variant. It originates from a point mutation in the human β-globin locus and is one of the most common hemoglobin variants worldwide.[1] It is so named because of its higher prevalence in the Punjab region of India and Pakistan, along with northern China, and North America. It is also the most frequent hemoglobin variant in Xinjiang Uyghur Autonomous Region of China, with a 1997 study indicating that Hemoglobin D-Punjab accounts for 55.6% of the total hemoglobin variants.[2]
Hemoglobin D is a result of a mutation in the one or both of the Beta-chains that make up hemoglobin molecules. Having one gene effected is referred to as trait; having two is referred to as homozygous "disease" although the symptoms of this disease are mild.
History
Until the early 1950s, hemoglobin A and some of its variants had been identified, such as hemoglobin S and hemoglobin C. Hemoglobin D was discovered in 1951 with one source stating it was the third variant discovered,[2] and another source claiming it was the fourth.[1] Later in 1962, it was found that five other regional variants of hemoglobin D all had the same chemical structure termed hemoglobin D-Punjab.[1]
Hemoglobin D Trait
Hemoglobin is the main ingredient in red blood cells. Hemoglobin helps red blood cells carry oxygen from the lungs to other parts of the body. Normal red blood cells have hemoglobin A. People with hemoglobin D trait have red blood cells that have normal hemoglobin A (made up of normal alpha and beta chains) and abnormal hemoglobin D (made up of normal alpha chains and variant beta chains). People with hemoglobin D trait have slightly more hemoglobin A than hemoglobin D. The abnormal hemoglobin is called hemoglobin D.[3]
People with Hemoglobin D trait do not have health problems related to having the trait. People with hemoglobin D trait do not have Hemoglobin D disease or sickle cell disease. They cannot develop these diseases later in life. While Hemoglobin D can be detected without a DNA test, one is needed to ascertain that a person who carries Hemoglobin D carries hemoglobin D-Punjab.[citation needed]
There is no clinical disease detected, however children of affected individuals have increased risk of having Hemoglobin D Disease, Hemoglobin SD disease or Beta-thalassemia Disease.[citation needed] Among the seven known types of Hemoglobin D, only Hemoglobin D Punjab can cause a serious hemoglobin disorder.
Symptoms
usually present with mild hemolytic anemia and mild to moderate splenomegaly.
Even homozygous Hemoglobin D disease does not typically cause clinically significant symptoms. It is usually present with mild haemolytic anaemia and moderate splenomegaly.[4] The anemia usually occurs in the first few months of life, as fetal hemoglobin decreases and hemoglobin D increases.[citation needed]
Hb D-Punjab becomes significant when it is co-inherited with Hb S or B thalassemia.
See also
References
- ^ a b c d Torres, Lidiane de Souza; Okumura, Jéssika Viviani; Silva, Danilo Grünig Humberto da; Bonini-Domingos, Claudia Regina (March 2015). "Hemoglobin D-Punjab: origin, distribution and laboratory diagnosis". Revista Brasileira de Hematologia e Hemoterapia. 37: 120–126. doi:10.1016/j.bjhh.2015.02.007. ISSN 1516-8484.
- ^ a b c El-Kalla, S.; Mathews, A. R. (January 1997). "HB D-Punjab in the United Arab Emirates". Hemoglobin. 21 (4): 369–375. doi:10.3109/03630269709000669. ISSN 0363-0269.
- ^ "Hemoglobin D Trait".
- ^ Pandey, Sanjay; Mishra, Rahasya Mani; Pandey, Sweta; Shah, Vineet; Saxena, Renu (2012). "Molecular characterization of hemoglobin D Punjab traits and clinical-hematological profile of the patients". Sao Paulo Medical Journal. 130: 248–251. doi:10.1590/S1516-31802012000400008. ISSN 1516-3180.
1. Tyagi S, Marwaha N, Parmar V, Basu S. Sickle cell hemoglobin-D Punjab disease (Compound Heterozygous state). Ind J Hematol Blood Transf 2000;18:31-2. 2. Zeng YT, Huang SZ, Ren ZR, Li HJ (1989). "Identification of Hb D-Punjab gene: application of DNA amplification in the study of abnormal hemoglobins". Am. J. Hum. Genet. 44 (6): 886–9. PMC 1715661. PMID 2729278. 3. http://www.idph.state.il.us/HealthWellness/fs/hemoglobin_d.htm 4. http://health.utah.gov/newbornscreening/Disorders/HB/Hb_D_Disease_DD/FactSheet_Provider_HbDD_En.pdf 5. www.chime.ucl.ac.uk/APoGI/data/rtf/hb/carriers/b/dp/carbook.rtf