MSK deformities Flashcards
What are the most common forms of skeletal dysplasia
Achondroplasia
Hypochondroplasia
What is the aetiology of achondroplasia
Autosomal dominant BUT 70% sporadic mutations in fibroblast growth factor receptor 3 (FGFR3)
What are the signs and symptoms of achondroplasia
Short stature, shortening of limbs (Rhizomelia), ± hydrocephalus
Large head, frontal bossing
Depression of nasal bridge
Short, broad hands
Marked lumbar lordosis
‘Trident Hands’
Define dwarfism
height less than 2 S.D. below the mean
What are the signs and symptoms of hypochondroplasia
Small stature
Micromelia (small extremities)
Large head
What is SHOX
Short stature homeobox gene
Seen in Turner’s (1 less) and klinefelters (>2 SHOX)
X-linked
What is osteogenesis imperfecta
S/S: blue sclera, short stature, loose joints, hearing loss, breathing problems
Types = 7 forms
- Most common: type 1 = abnormal pro-alpha 1 or 2 collagen polypeptides
What investigations should be done for achondroplasia
Prenatal scans (not apparent until more than 22w GA so may be missed)
Clinical diagnosis (and XR findings)
- Metaphyseal irregularity (inverted V metaphysis = ‘chevron deformity’
- Flaring in long bones, late-appearing irregular epiphyses
Molecular analysis confirmation
What are the complications of achondroplasia
Gross motor skill delay
Kyphosis
Early osteoarthritis
Risks from hydrocephalus
Obesity
ENT issues