Standard pre‑examination protocol – must be demonstrated:
Action: Introduce yourself, explain the examination, and obtain verbal consent.
Key observations – “Bell’s palsy” clues:
Focused cranial nerve examination – differentiate UMN vs LMN:
Systematic examination – identify aetiology & complications:
Assess:
📋 Case Presentation – (fill in during exam)
This is a _____-year-old _____ child, referred for _____ (acute facial weakness / drooling / eye closure difficulty). On examination, the child appears _____ (well / unwell), with _____ (unilateral facial weakness / bilateral). Forehead: _____ (wrinkling lost / preserved). Eye closure: _____ (incomplete / complete). Mouth: _____ (drooping / pulling to normal side). Ear: _____ (vesicles / normal). Cranial nerves: V _____, IX/X _____, XII _____. Tone & reflexes: _____ (normal / hemiparesis). GPE: _____ (rash / lymphadenopathy / parotid swelling). Growth: weight _____ percentile, length _____ percentile.
• Bell’s palsy (idiopathic) – most common (HSV-1 reactivation).
• Ramsay Hunt syndrome – herpes zoster oticus (vesicles, ear pain).
• Lyme disease – bilateral facial palsy, rash, arthritis.
• Acute otitis media / mastoiditis – ear pain, fever.
• Parotid tumour / infection – swelling, pain.
• Trauma – temporal bone fracture, birth trauma.
• Guillain-Barré syndrome – bilateral facial palsy with ascending weakness.
• Sarcoidosis – bilateral, other cranial nerves.
• Brainstem stroke / tumour – UMN signs, other deficits.
• Congenital – Möbius syndrome (bilateral, with other CN palsies).
• Clinical diagnosis – typical presentation: acute unilateral LMN VII palsy.
• Lyme serology: if endemic or bilateral.
• HSV/VZV PCR: if vesicles (Ramsay Hunt).
• MRI brain / IAC: if atypical (slow onset, recurrent, other CN).
• EMG / NCS: if prognosis needed (after 1 week).
• Lyme serology (ELISA + Western blot): if exposure/tick bite.
• VZV PCR (vesicle fluid): Ramsay Hunt.
• Sarcoidosis: ACE, chest X‑ray.
• HIV: if risk factors.
• CSF: if meningitis or other CN involvement.
• MRI brain + IAC: exclude tumour, stroke, demyelination.
• Audiometry: if hearing loss (exclude acoustic neuroma).
• CT temporal bone: if trauma or mastoiditis.
• CSF: if suspect GBS, meningitis, sarcoidosis.
• Ophthalmology assessment: corneal exposure, ulceration.
• Electroneuronography (ENoG): if >90% degeneration at 2 weeks → poor prognosis.
• Schirmer’s test: reduced tearing (if greater petrosal nerve involved).
• Synkinesis assessment: at follow-up.
🔹 Management – Across Organ Systems
Prednisolone (1 mg/kg/day × 7‑10 days) if within 72 hours. Acyclovir if Ramsay Hunt or severe.
Artificial tears, eye patch at night, tape eyelid closed. Ophthalmology referral.
Soft diet if chewing difficulty. Monitor for aspiration.
Facial massage, exercises to prevent synkinesis and muscle atrophy.
Counselling, school support for facial appearance, self-esteem.
Neurology, ophthalmology, physiotherapy, speech therapy, psychology.
📈 Prognosis
📋 Follow‑up Schedule