46,XY disorder of sex development due to isolated 17, 20 lyase deficiency (Q91110): Difference between revisions
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Refere-se a distúrbio do desenvolvimento sexual devido a um raro transtorno genético endócrino e autossômico recessivo que é caracterizado por uma perda completa ou parcial da atividade da 17,20-liase e, por sua vez, produção comprometida de estrogênios sexuais e de androgênios sexuais. | |||
| description / en | description / en | ||
This refers to disorder of sex development due to a rare endocrine and autosomal recessive genetic disorder which is characterised by a complete or partial loss of 17,20-lyase activity and, in turn, impaired production of the androgen and estrogen sex steroids. | |||
Revision as of 18:06, 15 August 2026
This refers to disorder of sex development due to a rare endocrine and autosomal recessive genetic disorder which is characterised by a complete or partial loss of 17,20-lyase activity and, in turn, impaired production of the androgen and estrogen sex steroids.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_513865687 |
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| English | 46,XY disorder of sex development due to isolated 17, 20 lyase deficiency |
This refers to disorder of sex development due to a rare endocrine and autosomal recessive genetic disorder which is characterised by a complete or partial loss of 17,20-lyase activity and, in turn, impaired production of the androgen and estrogen sex steroids. |
