A. Autosomal dominant
B. Autosomal recessive
C. Se* linked recessive
D. Not a inheritable trait
Related Mcqs:
- Clinical evidence of dentinogenesis imperfecta is______________?
A. Defective enamel and dentine
B. Defective dentine and obliterated pulp chamber
C. Increased rate of caries
D. Oligodontia - Dentinogensis imperfecta differs from amelogenesis imperfecta in that, the former is_____________?
A. A hereditary disturbance
B. The result of excessive fluoride ingestion
C. The result of faulty enamel matrix formation
D. Characterized by calcification of pulp chambers and the root canals of the teeth - Shell teeth are more common in this variant of dentinogenesis imperfecta________________?
A. Type I
B. Type III
C. Type II
D. Type IIII and I - Amelogenesis imperfecta is a disorder of_____________?
A. Ectoderm
B. Mesoderm
C. Endoderm
D. Ecto and Mesoderm - The inheritance pattern of dentinogensis imperfecta is______________?
A. Homozygous
B. Autosomal dominant
C. Recessive
D. X-linked recessive - Dentinogenesis by odontoblasts first begins at_____________?
A. Pulpal end
B. Cusp tip
C. Tooth bud stage
D. Cervical area - Biochemical abnormality associated with osteogenesis imperfecta is increase in______________?
A. Alkaline phosphatase
B. Acid phosphatase
C. Bicarbonate ion
D. Phosphorylase enzyme - A 15-year old boy shows an inverted pear shaped radiolucency between the upper central incisors. The teeth are normal in all aspects The most likely diagnosis is________________?
A. Globulomaxillary cyst
B. Nasopalatine cyst
C. Aneurysmal cyst
D. Dentigerous cyst - The 2nd common most supernumerary teeth is________________?
A. Mesiodens
B. Distal to 3rd molar in maxilla
C. Distal to mandibular 3rd molar
D. Para molars - The cyst located at the junction of medial nasal process, lateral nasal process and maxillary process is________________?
A. Globulomaxillary cyst
B. Median palatine cyst
C. Nasopalatine cyst
D. Nasoalveolar cyst
