A. symptoms are similar
B. life long immunity results
C. vesicles occur with both diseases
D. intranuclear inclusion bodies are present
Related Mcqs:
- The reason why most patients suffering from recurrent herpes labialis rarely give a history of having acute form of the herpetic gingivastomatitis is because_____________?
A. Etiological agents differ
B. The acute form occurs only inversely immuno compromised individuals
C. The primary infection was subclinical
D. The patient has received antibodies during intrauterine life and the antibodies have persisted - Recurrent herpes occurs due to_______________?
A. Virus in oral mucosa
B. Latent virus is skin supplying the area
C. Latent virus in nerve ganglia
D. None of the above - The bacteria observed as a causative organism in case of Recurrent apthous ulcers is __________________?
A. Streptococcus sangius
B. Streptococcus mutans
C. Borellia vincentii
D. Staphylococci albus - For primary herpes simplex, the diagnosis is made by which gene______________?
A. Culture with giemsa stain:
B. Culture with wright strain
C. Routing cytology
D. Flourescent stain for cytology - The feature that distinguishes herpes zoster from other vesiculo bullous eruption is_____________?
A. Unilateral occurrence
B. Severe burning pain
C. Prominent crusting vesicles
D. Sub epidermal bullous formation - Herpes simplex is seen in______________?
A. < 10 yrs. of age
B. 12-15 yrs. of age
C. 25-30 yrs. of age
D. 55-60 yrs. of age - Recurrent ulcers occurring on gingiva and palate are most probably________________?
A. Aphthous ulcers
B. Herpes simplex
C. koplick spots
D. Lesions of Behcet’s syndrome - Which is best for diagnosis of primary herpes simplex infection ?
A. Smear stained with Giemsa stain
B. Smear stained with Wrist’s stain
C. Flurorescent staining of cytology smear
D. Routing cytology - A 7-year old child having yellowish discoloured spot of maxillary central incisor. His mother presents a history of injury to deciduous tooth 3 years back with recurrent infection & swelling. The diagnosis is_______________?
A. Turners hypoplasia
B. Generalised dental fluorosis
C. Syphillitic hypoplasia
D. Rickets hypomineralisation - 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
