Hyperhomocysteinaemia (Q39593): Difference between revisions
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Doença causada por deficiências de vitaminas B6, ácido fólico ou vitamina B12. Os defeitos genéticos da 5-MTHF redutase podem consequentemente levar à hiperhomocisteinemia. Esta doença é caracterizada por níveis anormalmente elevados de homocisteína no sangue. Esta doença pode se manifestar com doença cardiovascular, trombose, esquizofrenia e osteoporose. A confirmação é pela identificação da deficiência em uma amostra de sangue | |||
| description / en | description / en | ||
A disease caused by deficiencies of vitamin B6, folic acid, or vitamin B12. Genetic defects in 5-MTHF reductase can consequently lead to hyperhomocysteinaemia. This disease is characterised by abnormally high level of homocysteine in the blood. This disease may present with cardiovascular disease, thrombosis, schizophrenia and osteoporosis. Confirmation is by identification of deficiency in a blood sample. | |||
Revision as of 05:04, 13 August 2026
A disease caused by deficiencies of vitamin B6, folic acid, or vitamin B12. Genetic defects in 5-MTHF reductase can consequently lead to hyperhomocysteinaemia. This disease is characterised by abnormally high level of homocysteine in the blood. This disease may present with cardiovascular disease, thrombosis, schizophrenia and osteoporosis. Confirmation is by identification of deficiency in a blood sample.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3B61.00 |
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| English | Hyperhomocysteinaemia |
A disease caused by deficiencies of vitamin B6, folic acid, or vitamin B12. Genetic defects in 5-MTHF reductase can consequently lead to hyperhomocysteinaemia. This disease is characterised by abnormally high level of homocysteine in the blood. This disease may present with cardiovascular disease, thrombosis, schizophrenia and osteoporosis. Confirmation is by identification of deficiency in a blood sample. |
