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प्रश्न
Differentiate between Mendelian and Chromosomal disorders.
अंतर स्पष्ट करें
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उत्तर
| Basis | Mendelian disorders | Chromosomal disorders |
| Cause | Mutation in a single gene (altered allele). | Abnormal number or structure of whole chromosomes (aneuploidy, deletions, translocations). |
| Pattern of inheritance | Follows Mendel’s single‑gene patterns dominant, recessive or sex‑linked. | Usually not simple Mendelian; often sporadic (e.g., from meiotic nondisjunction) and may not show typical parent‑to‑child Mendelian ratios. |
| Example | Cystic fibrosis, sickle cell single‑gene inheritance. | Down syndrome (trisomy 21) caused by nondisjunction leading to an extra chromosome. |
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2025-2026 (March) 57-1-3
