A. Rickets
B. Osteogenesis imperfecta
C. Osteomyelitis
D. Osteoma
Related Mcqs:
- A 20yr old patient reports with multiple swelling of the jaws. Clinical examination reveals multiple hard swellings involving the jaws and intra orally several missing teeth are noticed. Panoramic radiograph reveals multiple radio opaque lesions in the maxilla and the mandible with multiple impacted teeth and supernumerary teeth indicative of Gardeners syndrome: The above mentioned condition is______________?
A. Autosomal dominant disease
B. Autosomal recessive disorder
C. X-linked disease
D. A syndrome of unknown cause - The type of embolism seen in fractures of long bones_____________?
A. Thrombo embolism
B. Air embolism
C. Fat embolism
D. Amniotic fluid embolism - Amber coloured tooth traslucency, blue sclerae and bone fragility and a history of pervious bone fractures are characteristic findings in_____________?
A. Osteoporosis
B. Osteogenesis imperfecta
C. Osteitis deformans
D. Osteitis fibrosa cystic - A 10-years-old child presents with anemia and recurrent fractures. The X-ray shows diffuse hyper density of bone The diagnosis is most likely to be______________?
A. Osteogenesis imperfecta
B. Osteopetrosis
C. Osteochondroma
D. Hyperparathyroidism - Multiple osteomas, multiple polyposis, supernumerary teeth are found in _______ syndrome?
A. Reiter’s
B. Peutz – jeghers
C. Gardner’s
D. Behcet’s - Bifid ribs, multiple radiolucent lesions of the jaws multiple basal cell nevi and flax cerebri calcification are found in:_____________?
A. Basal cell nevus syndrome
B. Sturge weber syndrome
C. Horner syndrome
D. Hereditary internal polyposis - Bone pain, bone, cyst, fractures and renal stones are characteristics of_____________?
A. Hyperparathyroidism
B. Cushing’s syndorme
C. Multiple myeloma
D. Marfan’s syndrome - Incomplete fractures of the bone are called___________?
A. Comminuted fracture
B. Compound fracture
C. Simple fracture
D. Green stick fracture - Delayed dentition with multiple supernumerary teeth is seen in________________?
A. Hypoparathyroidism
B. Cleidocranial dysplasia
C. Pierre Robin Syndrome
D. Mongolism (Down’s Syndrome - Cotton-wool appearance is seen in______________?
A. Peget’s disease
B. Osteoclerosis
C. Pariapical cemential dysplasia
D. Ossifying fibroma