Certain human genetic disorders are due to a single affected or mutated allele or specific chromosomal changes, such as nondisjunction. These disorders include Sickle cell anemia, Tay-Sachs disease, Huntington's disease, X-linked color blindness, Trisomy 21 (Down syndrome), Triple X syndrome, and Turner Syndrome.
Alcuni disturbi genetici umani sono dovuti a un singolo allele colpito o mutato o a specifici cambiamenti cromosomici, come la nondisgiunzione. Questi disturbi includono l'anemia falciforme, la malattia di Tay-Sachs, la malattia di Huntington, il daltonismo legato all'X, la Trisomia 21 (sindrome di Down), la sindrome della tripla X e la sindrome di Turner.
| Text | Certain human genetic disorders are due to a single affected or mutated allele or specific chromosomal changes, such as nondisjunction. These disorders include Sickle cell anemia, Tay-Sachs disease, Huntington's disease, X-linked color blindness, Trisomy 21 (Down syndrome), Triple X syndrome, and Turner Syndrome. |
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