Osteogenesis imperfecta_____________?

Related Mcqs:

1. Biochemical abnormality associated with osteogenesis imperfecta is increase in______________?

   A. Alkaline phosphatase
   B. Acid phosphatase
   C. Bicarbonate ion
   D. Phosphorylase enzyme

2. Which of the following are a triad of the sign and symptoms of osteogenesis imperfecta________________?

   A. blue sclera, sparse hair, anhydrosis
   B. enlarged hand, feet, maxilla, mandible
   C. Blue sclera, brittle bones opalescent dentin
   D. blue sclera, arachnodactyly, brittle bones

3. The primary causative factor for myofacial pain dysfunction syndrome of the TMJ is_______________?

   A. Infratemporal space infection
   B. Auriculotemporal neuritis
   C. Muscular overextension and over contraction
   D. Otitis media

4. 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

5. In Cleidorcranial dysostosis, sometimes the roots of the permanent teeth are_____________?

   A. Thin and long
   B. thin and short
   C. Thick and short
   D. Fused

6. A patient aged 50 years presented with a history of jaw expansion and enlargement of maxilla_____________?

   A. paget’s disease
   B. Acromegaly
   C. Fibrous dysplasia
   D. Hyperparathyroidism

7. Histopathologically reversal lines are seen in_____________?

   A. Cherubism
   B. Fibrous dysplasia
   C. Paget’s disease of the bone
   D. Craniofacial dysplasia

8. Delayed dentition with multiple supernumerary teeth is seen in________________?

   A. Hypoparathyroidism
   B. Cleidocranial dysplasia
   C. Pierre Robin Syndrome
   D. Mongolism (Down’s Syndrome

9. Delayed eruption of teeth occurs in_________________?

   A. Craniofacial dysostosis
   B. Hyperthyroidism
   C. Cleidocranial dysostosis
   D. Osteitis deformans

10. Precocious puberty is most characteristic of which of the following ?

    A. Jaffe’s syndrome
    B. Monostotic fibrous dysplasia
    C. Abright’s syndrome
    D. Osteogenesi imperfecta