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Cerebral palsy, tics and dystonia are in Set 7; Guillain-Barré syndrome and myasthenia in Set 6.
Case Complete
What this deck covers
Neurology – Set 8 in 50 board-style clinical cases with worked explanations. Each case gives you a clinical vignette, four options, the correct answer, and an explanation of why each of the other three is wrong, with the guideline or textbook it follows named on the answer.
Board-style teaching questions for paediatricians and trainees preparing for paediatric board, MRCPCH and licensing examinations. Written from published guidelines and standard paediatric textbooks, with the source named on every answer.
The 50 cases, in order
- Floppy, bright-eyed infant
- How he gets up from the floor
- Girl losing hand use and words
- New motor signs on levodopa
- Unsteady boy with red-eye vessels
- Before daily prednisolone starts
- Floppy baby with gastroenteritis
- Pigmented gums, slipping school marks
- School decline, rigidity and seizures
- Parents ask how severe it will be
- Boy slow to release his grip
- Weak, alert baby with no reflexes
- Late walker with big firm calves
- Parents fear sudden death
- Cold in a weak 5-month-old
- Long-term risk parents ask about
- Fidgety girl, a sign to look for
- School decline and tanned skin
- Why her illness began so young
- Third chest infection this year
- Affected boy, affected uncle
- Toe-walking girl with dystonia
- Frog-leg posture, absent reflexes
- Motor plateau at 6 years
- Chance of it happening again
- Girl who cannot let go of a handle
- Low cortisol before sedation
- Mother plans another pregnancy
- Back pain after slipping off a step
- Wobbly since her first steps
- Long PR interval and a slow handshake
- Grandmother asks about polio
- Leaning to one side in her chair
- Bright baby with a rippling tongue
- Abnormal liver tests, frequent falls
- Missing objects in the lower fields
- Head lag after the diarrhoea settles
- Cramps but still playing football
- Transplant question from parents
- Yearly review of a sleepy teenager
- What else comes with her ataxia
- A year after he stopped walking
- A second white-matter disease
- Well newborn with an affected sister
- Flickering tongue, absent reflexes
- Slow to run, with a very high CK
- How juvenile Batten disease begins
- Morning headaches at 14
- Untreated natural history
- Tripping from weak ankles
Diagnoses and management options tested
Across the fifty cases you are asked to choose between options such as: Congenital muscular dystrophy, Rhythmic oscillation at a steady frequency, Discharge once drinking, with no further tone review, Degree of denervation on EMG, Myotonic dystrophy type 1, Cerebellar medulloblastoma, Two mutant copies, one from each parent, Caudate head atrophy with boxy ventricles, About 25%, as both parents are carriers, Any affected child will be milder than she is, CTG repeat sizing in the DMPK gene, Neurogenic pattern on electromyography, It is a normal variant; reassure and discharge him, Renal ultrasound to look for kidney stones.
Clinical pearls from this deck
- Floppy, areflexic, fasciculating but bright-eyed: think of spinal muscular atrophy.
- Hands on the thighs to stand means weak hips, whatever the cause.
- Lost hand use plus hand-wringing in a regressing girl is Rett syndrome until proved otherwise.
- Chorea flows, tremor oscillates, dystonia twists, and tics follow an urge.
- Ataxia first, telangiectasia a few years later, infections throughout.
- Before steroids, close the chickenpox gap.
Work through the deck once for recognition, then again a week later to test yourself — each question gives the answer and explains why every other option fails.
More from this system: all neurology case decks · pediatric reference values.