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T21 – SÍNDROME DE DOWN: O QUE É? A Síndrome de Down, também chamada de Trissomia do cromossomo 21 , é uma condição genética caracterizada pela presença de três cópias do cromossomo 21, em vez de duas. Essa alteração ocorre ainda na formação do embrião e não é uma doença, nem resultado de escolhas dos pais. Existem três tipos de Síndrome de Down: • Trissomia simples • Translocação • Mosaicismo Cada uma pode influenciar o desenvolvimento de forma diferente, reforçando que nã
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