Atypical Werner syndrome (Q97577): Difference between revisions
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Síndrome de Werner atípica refere-se a um grupo heterogêneo de casos que são clinicamente diagnosticados como síndrome de Werner (WS), mas não são portadores de mutações genéticas WRN. De forma similar à WS clássica causada por mutações WRN, geralmente exibem uma aparência envelhecida e transtornos comuns relacionados à idade em idades mais precoces quando comparados à população em geral. | |||
| description / en | description / en | ||
Atypical Werner syndrome refers to a heterogeneous group of cases that are clinically diagnosed as Werner syndrome (WS; ) but do not carry WRN gene mutations. Similar to classical WS caused by WRN mutations, they generally exhibit an aged appearance and common age-related disorders at earlier ages compared to the general population. | |||
Revision as of 13:41, 16 August 2026
Atypical Werner syndrome refers to a heterogeneous group of cases that are clinically diagnosed as Werner syndrome (WS; ) but do not carry WRN gene mutations. Similar to classical WS caused by WRN mutations, they generally exhibit an aged appearance and common age-related disorders at earlier ages compared to the general population.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1661142154 |
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| English | Atypical Werner syndrome |
Atypical Werner syndrome refers to a heterogeneous group of cases that are clinically diagnosed as Werner syndrome (WS; ) but do not carry WRN gene mutations. Similar to classical WS caused by WRN mutations, they generally exhibit an aged appearance and common age-related disorders at earlier ages compared to the general population. |
