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hyperhomocysteinémia

Č. záznamu	d020138
Dátum	06.06.2025
Typ	M - MESH
Tematický termín	hyperhomocysteinémia
Iný termín	Slovenčina (Pseudonym) hyperhomocystinémia Slovenčina (Pseudonym) hyperhomocysteinaemia Slovenčina (Pseudonym) hyperhomocystinaemia
MDT	C16.320.565.100.480C18.452.603.378C18.452.648.100.480C18.654.521.500.133.699.418
Poznámka	Condition in which the plasma levels of homocysteine and related metabolites are elevated (>13.9 μmol/l). Hyperhomocysteinemia can be familial or acquired. Development of the acquired hyperhomocysteinemia is mostly associated with vitamins B and/or folate deficiency (e.g., PERNICIOUS ANEMIA, vitamin malabsorption). Familial hyperhomocysteinemia often results in a more severe elevation of total homocysteine and excretion into the urine, resulting in HOMOCYSTINURIA. Hyperhomocysteinemia is a risk factor for cardiovascular and neurodegenerative diseases, osteoporotic fractures and complications during pregnancy.

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