Which inheritance pattern explains maternal transmission of a mitochondrial disorder?

Prepare for the NBME Form 16 with our comprehensive quiz. Tackle multiple choice questions with insights and explanations. Enhance your confidence and accuracy for the exam!

Multiple Choice

Which inheritance pattern explains maternal transmission of a mitochondrial disorder?

Explanation:
Mitochondrial disorders show maternal transmission because mitochondria and their DNA come from the mother through the egg’s cytoplasm. Each child inherits the mother’s mitochondrial DNA, so an affected mother can pass the mutation to all of her children (both sons and daughters), while fathers do not pass mitochondria to their offspring. The severity among offspring can vary because cells can contain a mix of normal and mutated mitochondria (heteroplasmy), leading to different clinical expressions even within the same family. This pattern stands in contrast to autosomal dominant, X-linked recessive, or Y-linked inheritance, which involve different transmission routes and would not produce this strictly maternal pattern.

Mitochondrial disorders show maternal transmission because mitochondria and their DNA come from the mother through the egg’s cytoplasm. Each child inherits the mother’s mitochondrial DNA, so an affected mother can pass the mutation to all of her children (both sons and daughters), while fathers do not pass mitochondria to their offspring. The severity among offspring can vary because cells can contain a mix of normal and mutated mitochondria (heteroplasmy), leading to different clinical expressions even within the same family. This pattern stands in contrast to autosomal dominant, X-linked recessive, or Y-linked inheritance, which involve different transmission routes and would not produce this strictly maternal pattern.

Subscribe

Get the latest from Passetra

You can unsubscribe at any time. Read our privacy policy