Sickle cell Hb-C disease without crisis (Q68828): Difference between revisions
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| description / pt-br | description / pt-br | ||
Doença causada pela herança de uma mutação da HbS de um progenitor e de uma mutação da HbC do outro progenitor. Esta doença é caracterizada por hemácias em forma de foice rígidas e anormais na ausência de crise. Esta doença pode se manifestar com fadiga, falta de ar, tonturas, dores de cabeça, palidez de pele ou mucosas e icterícia. Esta doença é confirmada por identificação de mutação da HbS e da HbC por meio de testes genéticos. | |||
| description / en | description / en | ||
A disease caused by the inheritance of a HbS mutation from one parent and a HbC mutation from the other parent. This disease is characterised by abnormal rigid sickle-shaped red blood cells in the absence of crisis. This disease may present with fatigue, shortness of breath, dizziness, headaches, pallor of skin or mucous membranes, and jaundice. This disease is confirmed by identification of HbS and HbC mutation by genetic testing. | |||
Revision as of 16:54, 14 August 2026
A disease caused by the inheritance of a HbS mutation from one parent and a HbC mutation from the other parent. This disease is characterised by abnormal rigid sickle-shaped red blood cells in the absence of crisis. This disease may present with fatigue, shortness of breath, dizziness, headaches, pallor of skin or mucous membranes, and jaundice. This disease is confirmed by identification of HbS and HbC mutation by genetic testing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_135961609 |
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| English | Sickle cell Hb-C disease without crisis |
A disease caused by the inheritance of a HbS mutation from one parent and a HbC mutation from the other parent. This disease is characterised by abnormal rigid sickle-shaped red blood cells in the absence of crisis. This disease may present with fatigue, shortness of breath, dizziness, headaches, pallor of skin or mucous membranes, and jaundice. This disease is confirmed by identification of HbS and HbC mutation by genetic testing. |
