Free Oral Manifestations of Systemic Disease MCQs with Answers

309 Oral Manifestations of Systemic Disease MCQs from Oral Pathology and Medicine, each with the correct answer and a written explanation of why it is correct. Free and unlimited, with no account needed.

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309 questions · page 4 of 16

  • A. Rickets
  • B. Osteoma
  • C. Osteomyelitis
  • D. Osteogenesis imperfecta

Explanation: Osteogenesis imperfecta causes defective type I collagen, making bones brittle and prone to recurrent or multiple fractures.

Correct answer: Osteogenesis imperfecta
  • A. Temporalis
  • B. Lateral pterygoid
  • C. Masseter
  • D. Buccinator

Explanation: In myofascial pain dysfunction syndrome, the lateral pterygoid is a frequently involved muscle and may show marked tenderness or spasm.

Correct answer: Lateral pterygoid
  • A. Pagets disease
  • B. Weing's sarcoma
  • C. Fibrous dysplasia
  • D. Osteosarcoma

Explanation: Fibrous dysplasia replaces normal bone with cellular fibrous tissue and immature woven bone, producing a ground-glass or orange-peel…

Correct answer: Fibrous dysplasia
  • A. Hypoparathyroidism
  • B. Mongolism (Down's Syndrome
  • C. Pierre Robin Syndrome
  • D. Cleidocranial dysplasia

Explanation: Cleidocranial dysplasia characteristically causes delayed eruption of permanent teeth together with numerous unerupted supernumerary teeth…

Correct answer: Cleidocranial dysplasia
  • A. paget's disease
  • B. fibrous dysplasia
  • C. Osteopetrosis
  • D. Osteogenesis imperfecta

Explanation: Paget disease produces a mosaic or “jigsaw puzzle” pattern histologically and may show a cotton-wool appearance radiographically.

Correct answer: paget's disease
  • A. Synovial chondromatosis
  • B. Ankylosis
  • C. Subluxation
  • D. Osteorthritis

Explanation: Rheumatoid inflammation of the TMJ can progressively destroy the articular surfaces and lead to fibrous or bony ankylosis, a classic…

Correct answer: Ankylosis
  • A. Maxillary prognathism
  • B. Mandibular retrognathia
  • C. Maxillary hypoplasia
  • D. Mandibular prognathism

Explanation: Down syndrome commonly produces midface and maxillary hypoplasia, with a flat nasal bridge and the appearance of relative mandibular…

Correct answer: Maxillary hypoplasia
  • A. Maxillofacial Dysostosis
  • B. Condylar Dysostosis
  • C. Maxillomandibulofacial Dysostosis
  • D. Mandibulofacial Dysostosis

Explanation: Treacher Collins syndrome is also called mandibulofacial dysostosis, a developmental disorder involving the mandible, zygomas, maxilla and…

Correct answer: Mandibulofacial Dysostosis
  • A. Rendu-Osler-Weber disease
  • B. Maffuci's syndrome
  • C. Angioosteohypertrophy syndrome
  • D. Sturge weber syndrome

Explanation: Sturge-Weber syndrome is a neurocutaneous vascular disorder involving leptomeningeal angiomas, often with a facial port-wine stain and…

Correct answer: Sturge weber syndrome
  • A. Crouzon's syndrome
  • B. Apert's syndrome
  • C. Pierre robin syndrome
  • D. Down syndrome

Explanation: Apert syndrome is an acrocephalosyndactyly syndrome marked by craniosynostosis, abnormal digit development such as polydactyly or…

Correct answer: Apert's syndrome
  • A. Osteopetrosis
  • B. Osteogenesis imperfecta
  • C. Osteitis deformans
  • D. Acromegaly

Explanation: Paget disease, also called osteitis deformans, carries an increased risk of secondary osteosarcoma.

Correct answer: Osteitis deformans
  • A. Cherubism
  • B. Fibrous dysplasia
  • C. Craniofacial dysplasia
  • D. Paget's disease of the bone

Explanation: Paget disease shows a mosaic pattern of bone remodeling, with prominent reversal lines separating successive areas of resorption and…

Correct answer: Paget's disease of the bone
  • A. Osteosarcoma
  • B. Multiple Myeloma
  • C. Metastatic carcinoma
  • D. Ewing sarcoma

Explanation: Multiple myeloma is commonly regarded as the most frequent primary malignant tumor involving bone overall, although osteosarcoma is the…

Correct answer: Multiple Myeloma
  • A. Micrognathia
  • B. Retrognathia
  • C. Coloboma of lower eyelid
  • D. Glossoptosis

Explanation: Pierre-Robin syndrome is characterized by mandibular micrognathia or retrognathia, posterior displacement of the tongue called…

Correct answer: Coloboma of lower eyelid
  • A. Primary hyperparathyroidism
  • B. Phantom bone disease
  • C. Paget's disease
  • D. Osteopetrosis

Explanation: Osteopetrosis results from defective osteoclastic bone resorption, so normal eruption paths may remain blocked and teeth can fail to…

Correct answer: Osteopetrosis
  • A. Fibrous dysplasia
  • B. Ossifying fibroma
  • C. Focal cementoosseous dysplasia
  • D. Periapical cementoosseous dysplasia

Explanation: Fibrous dysplasia is commonly caused by postzygotic activating mutations of the GNAS gene, producing abnormal Gs-alpha signaling and…

Correct answer: Fibrous dysplasia
  • A. Pulse granuloma
  • B. Pannus
  • C. Baker's cyst
  • D. Immune granuloma

Explanation: A pannus is vascular inflammatory granulation tissue in rheumatoid arthritis that spreads over and progressively destroys the articular…

Correct answer: Pannus
  • A. Hyperparathyroidism
  • B. Acromegaly
  • C. Fibrous dysplasia
  • D. paget's disease

Explanation: Paget disease commonly affects older adults and can cause enlargement and expansion of the maxilla or mandible, sometimes producing…

Correct answer: paget's disease
  • A. Adult skeleton
  • B. Pubertal skeleton
  • C. Infantile skeleton
  • D. Prepubertal skeleton

Explanation: Paget disease is a chronic, progressive disorder of bone that occurs mainly in adults, especially older adults.

Correct answer: Adult skeleton
  • A. pagets disease and osteopetrosis
  • B. pagets disease and polyostotic fibrous dysplasia
  • C. Cherubism and Polyostotic fibrous dysplasia
  • D. Cherubism and pagets disease

Explanation: Osteosarcoma can arise as a secondary malignancy in Paget disease and, less commonly, in polyostotic fibrous dysplasia.

Correct answer: pagets disease and polyostotic fibrous dysplasia