NEETPGAI
FeaturesNEET PGFMGEINI-CETNewsBlogPricing
Log inStart Free
NEETPGAI

AI-powered NEET PG preparation platform. Master all 19 subjects with adaptive MCQs, AI tutoring, and spaced repetition.

Product

  • Features
  • Subjects
  • Previous Year Questions
  • NEET PG Preparation
  • FMGE Preparation
  • INI-CET Preparation
  • Compare
  • Pricing
  • Blog

Features

  • Adaptive MCQ Practice
  • AI Tutor
  • Mock Tests
  • Spaced Repetition

Resources

  • Exam News
  • Blog
  • Study Guides
  • NEET PG Updates
  • Contact & support

Legal

  • Privacy Policy
  • Terms of Service
  • Refund & Cancellation

Stay updated

© 2026 NEETPGAI. All rights reserved.
    SubjectsBiochemistryInborn Errors of Cobalamin Metabolism (cblC Defect)
    Pre-clinicalBiochemistry

    Inborn Errors of Cobalamin Metabolism (cblC Defect)

    1 MCQs in Biochemistry for NEET PG

    1 Hard
    Start Practicing

    Sample Questions

    hard

    A 5-year-old girl presents with progressive neurological decline, ataxia, and hepatosplenomegaly. Urine organic acid analysis reveals elevated methylmalonic acid and homocysteine. Serum cobalamin level is normal, but methylmalonic CoA mutase activity is severely reduced. Which of the following metabolic defects best explains the clinical and biochemical findings?

    Ready to test yourself?

    Test your Biochemistry knowledge with AI-powered MCQs and detailed explanations — no signup required to try.

    Practice Biochemistry MCQs

    Ready to master Inborn Errors of Cobalamin Metabolism (cblC Defect)?

    Sign up free and practice all 1 Inborn Errors of Cobalamin Metabolism (cblC Defect) MCQs with AI-powered explanations tailored to your performance.

    Create Free Account