Full 2L QBank
Pathology All India exam e2b93ee7

most common sign in any mitochondrial inheritence diseases?

A
ataxia
B
external ophthalmoplegia
C
psychosis
D
neurogenic weakness
High-Yield Explanation
Mitochondrial diseases * significant clinical and genetic heterogeneity * syndromic and non-syndromic * often multi-system diseases * onset between bih and senescence * a common cause a chronic morbidity and more prevalent than previously thought Common phenotypes in adults PEO-Progressive External Ophthalmoplegia (m/c) K55- Kearns Sayre Syndrome MERRF= Myoclonic Epilepsy with Ragged Red Fibers MELAS= (Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-like episodes) ref : robbins 10th ed

Related Pathology MCQs

Practice 2,00,000+ NEET PG Questions Free

Timed mock tests, mistake queue analytics, audio lectures & zero attempt limits on i❤️Exams.

Start Free Mock Test Now