Benign familial copper deficiency (Q83523): 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 | ||
Trata-se de transtorno hematológico e neurológico familiar benigno muito raro. A doença envolve uma deficiência nutricional do oligoelemento cobre. O cobre é onipresente e a necessidade diária é baixa, tornando a deficiência de cobre adquirida muito rara. A deficiência de cobre pode se manifestar em paralelo com a vitamina B12 e outras deficiências nutricionais. | |||
| description / en | description / en | ||
This is a benign familial very rare haematological and neurological disorder. The disease involves a nutritional deficiency in the trace element copper. Copper is ubiquitous and daily requirement is low making acquired copper deficiency very rare. Copper deficiency can manifest in parallel with vitamin B12 and other nutritional deficiencies . | |||
Revision as of 08:53, 15 August 2026
This is a benign familial very rare haematological and neurological disorder. The disease involves a nutritional deficiency in the trace element copper. Copper is ubiquitous and daily requirement is low making acquired copper deficiency very rare. Copper deficiency can manifest in parallel with vitamin B12 and other nutritional deficiencies .
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_580108812 |
||
| English | Benign familial copper deficiency |
This is a benign familial very rare haematological and neurological disorder. The disease involves a nutritional deficiency in the trace element copper. Copper is ubiquitous and daily requirement is low making acquired copper deficiency very rare. Copper deficiency can manifest in parallel with vitamin B12 and other nutritional deficiencies . |
