Sickle cell Hb-C disease with crisis (Q55346): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| 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 anormais rígidas em forma de foice, com sintomas dependendo da localização de acometimento. 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 and crisis, with symptoms depending on the site of involvement. 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 02:59, 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 and crisis, with symptoms depending on the site of involvement. 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_43465573 |
||
| English | Sickle cell Hb-C disease with 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 and crisis, with symptoms depending on the site of involvement. 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. |
