Hemoglobinopathy: Difference between revisions
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==Symptoms== | ==Symptoms== | ||
Common symptoms of hemoglobinopathy include:<ref>{{Cite journal | |||
| author = [[Elisabeth Kohne]] | |||
| title = Hemoglobinopathies: clinical manifestations, diagnosis, and treatment | |||
| journal = [[Deutsches Arzteblatt international]] | |||
| volume = 108 | |||
| issue = 31-32 | |||
| pages = 532–540 | |||
| year = 2011 | |||
| month = August | |||
| doi = 10.3238/arztebl.2011.0532 | |||
| pmid = 21886666 | |||
}}</ref> | |||
*Skeletal deformitie | |||
*Tumorous masses | |||
== Migration patterns == | == Migration patterns == | ||
== Common variants == | == Common variants == | ||
Revision as of 15:32, 30 August 2018
Template:Search infobox Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Hemoglobinopathy is a kind of genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin molecule. Most common hemoglobinopathies include sickle-cell disease.
Symptoms
Common symptoms of hemoglobinopathy include:[1]
- Skeletal deformitie
- Tumorous masses
Migration patterns
Common variants
- Hb S
- Hb C
- Hb E
- Hb D-Punjab
- Hb O-Arab
- Hb G-Philadelphia
- Hb Hasharon
- Hb Korle-Bu
- Hb Lepore
- Hb M
Hemoglobinopathy and evolution
de:Hämoglobinopathie nl:Hemoglobinopathie
- ↑ Elisabeth Kohne (2011). "Hemoglobinopathies: clinical manifestations, diagnosis, and treatment". Deutsches Arzteblatt international. 108 (31–32): 532–540. doi:10.3238/arztebl.2011.0532. PMID 21886666. Unknown parameter
|month=ignored (help)