MODY 2 syndrome (Q102304): Difference between revisions
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| description / pt-br | description / pt-br | ||
Isso se refere a uma forma hereditária de diabetes causada por mutações em um gene autossômico dominante (independente do sexo, ou seja, herdado de qualquer um dos pais), interrompendo a produção de insulina. Esta forma é devida a qualquer uma das várias mutações no gene GCK e representa 30% –70% dos casos de MODY. Hiperglicemia de jejum leve ao longo da vida e pequeno da glicemia aumento após sobrecarga de glicose são comuns. | |||
| description / en | description / en | ||
This refers to the hereditary form of diabetes caused by mutations in an autosomal dominant gene (sex independent, i.e. inherited from any of the parents) disrupting insulin production. This form is due to any of several mutations in the GCK gene. 30%–70% cases. Mild fasting hyperglycaemia throughout life. Small rise on glucose loading. | |||
Revision as of 19:14, 16 August 2026
This refers to the hereditary form of diabetes caused by mutations in an autosomal dominant gene (sex independent, i.e. inherited from any of the parents) disrupting insulin production. This form is due to any of several mutations in the GCK gene. 30%–70% cases. Mild fasting hyperglycaemia throughout life. Small rise on glucose loading.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_990655222 |
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| English | MODY 2 syndrome |
This refers to the hereditary form of diabetes caused by mutations in an autosomal dominant gene (sex independent, i.e. inherited from any of the parents) disrupting insulin production. This form is due to any of several mutations in the GCK gene. 30%–70% cases. Mild fasting hyperglycaemia throughout life. Small rise on glucose loading. |
