Category Archives: Musculoskeletal
MPS IV (MORQUIO-BRAILSFORD SYNDROME) Case 1
11 year old girl with short stature
PYLE’S DISEASE (FAMILIAL METAPHYSEAL DYSPLASIA)
Middle aged female patient with complaints of fracture right leg following a trivial trauma.
OSTEOPOIKILOSIS
Incidental finding in eight radiographs from seven patients ( both shoulder radiographs from same patient), investigated for other reasons.
OSTEOGENESIS IMPERFECTA
Fig .1 An aborted foetus (Antenatal diagnosis of osteogenesis imperfecta Type II) Fig. 2 An infant died immediatly after birth.Failed resuscictation Fig. 3 a-d Nine year old girl with blue sclera,laxity of joints and bony deformities Fig. 4 a-d 11 year old boy with repeated fractures and short stature Fig. 5 a-b Young child with repeated fractures,joint laxity and bowing of lower limb Fig. 6 a-b young boy with repeated fractures and bowing of long bones Fig. 7 a-d 35 year old male patient of short stature with gross deformity of skeleton
OSTEOPETROSIS (Albers-Schonberg Disease)
Eighteen year old female patient with clinical diagnosis of Anemia for investigation.
THANATOPHORIC DYSPLASIA
Fig 1 and 3 are still born foetuses and fig 2 aborted foetus at 20 weeks
CAMPOMELIC DYSPLASIA (CAMTOMELIC DYSPLASIA)
One day old baby with ambiguous genitalia-full term normal delivery-Antenal diagnosis -foetus with short, bowed limbs,probably campomelic dysplasia
CRANIOSTENOSIS
Eleven years old (fig.1 A&B) and Eight year old( fig.2) male siblings with complaints of progressive loss of vision. No other abnormalities noticed clinically in skeleton or other systems
PACHYDERMOPERIOSTOSIS (Primary Hypertrophic Osteoarthropathy)
Young male patient with hyperhydrosis and coarse features of face
MYOSITIS OSSIFICANS PROGRESSIVA (Munch Meyer’s disease)
A seventeen year old male patient ( Figs 1-4 ) and 14 year old girl child (Fig. 5 ) with progrssive limitation of mobility from early child hood.
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