πŸ“˜ Propionic Acidemia (Propionyl-CoA Carboxylase Deficiency)

Nelson Textbook of Pediatrics 22nd Ed β€” Section 105.6 (Organic Acidemias). PCCA/PCCB mutations β†’ propionic acid accumulation. Metabolic acidosis, ketosis, hyperammonemia, neutropenia, C3-carnitine elevation, basal ganglia stroke. Treatment: IV carnitine, protein restriction, liver transplantation.

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πŸ“‹ 30 Clinical Scenarios β€” Propionic Acidemia (FCPS level)

πŸ“‡ High‑Yield Review Cards (Propionic Acidemia)

🩺 Symptom‑Based Approach: Suspected Propionic Acidemia

Select a presentation for diagnostic clues.

πŸ“‹ Emergency & Long-term Management of Propionic Acidemia

    ⚑ Reflex Prompts β€” Clinical Decisions in Propionic Acidemia

    πŸ“– Summary: Propionic Acidemia β€” Nelson 22nd Ed