- (A) Autosomal dominant inheritance
- (B) Inability to repair sunlight induced damage to DNA
- (C) Irregular accemulation of melanin in the basal cell layer
- (D) Acanthosis of epithelium with elongation of rete ridges
Medical Mcqs
- (A) Alport syndrome
- (B) Ehlers-Danlos syndrome
- (C) Marfan syndrome
- (D) McArdle’s disease
- (A) Direct immunofluorescence
- (B) Tzanck smear
- (C) FNAC
- (D) Histopathology
- (A) Acanthomatous ameloblastoma
- (B) Branchial cleft cyst
- (C) Myxoma
- (D) Simple ameloblastoma
- (A) Basal cell nevus syndrome
- (B) Sturge weber syndrome
- (C) Horner syndrome
- (D) Hereditary internal polyposis
- (A) Mandibular moral region
- (B) Maxillary molar region
- (C) Mandibular premolar region
- (D) Maxillary premolar region
- (A) Supernumerary teeth
- (B) Radiolucent and radiopaque areas
- (C) Masses of calcified areas
- (D) Distinguishable tooth – like structures
- (A) Periapical cemental dysplasia
- (B) Familial cemental dysplasia
- (C) Benign cementoblastoma
- (D) Hypercementosis
- (A) Lateral periodontal cyst
- (B) Apical periodontal cyst
- (C) Gingival cyst of new born
- (D) Gingival cysts of adult
- (A) Transforms into dentigerous cyst
- (B) Regresses after eruption of the tooth
- (C) Is found in the place of the missing tooth
- (D) Is a type of dentigerous cyst
