Showing page 1 of 42 (370 total shorts)
— subject: "Oral Pathology"
#1Oral Pathology
Premature exfoliation of deciduous teeth is seen in hypophosphatasia.
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Premature exfoliation of deciduous teeth is seen in 1. Hypophosphatasia 2. Hypophosphataemia 3. Hyperphosphtasia 4. Hyperparathyrroidism
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#2Oral Pathology
Leukocytopenia can be seen in influenza, agranulocytosis, and liver cirrhosis.
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Leucocytopenia is seen in 1. Influenza 2. Agranulocytosis 3. Liver cirrhosis 4. All of the above
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#3Oral Pathology
Group 2 (Cleidocranial dysplasia, achondroplasia, craniofacial dysostosis) is characterized by relative/absolute mandibular prognathism. These conditions involve maxillary hypoplasia or underdevelopment, creating relative mandibular prognathism. Group 1 conditions (Treacher Collins, Pierre-Robin, Leontiasis ossea) are not typically associated with mandibular prognathism - Pierre-Robin has micrognathia, and Treacher Collins has mandibular hypoplasia.
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Which of the following group of diseases are characterized by relative/absolute mandibular prognathism 1. Treacher collins syndrome, Pierre-robin syndrome, Leontiasis ossea 2. Cleidocranial dysplasia, achondroplasia, craniofacial dyostosis 3. Both A and B 4. None of the above
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#4Oral Pathology
Mean exposure of radiation from a pantomograph is approximately 250 mR.
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Mean exposure of radiation from pantamograph is 1. 90 mR 2. 120 mR 3. 250 mR 4. 300 mR
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#5Oral Pathology
Down syndrome is characterized by large anterior fontanelles that close late, open sutures, slanting palpebral fissures (mongoloid), decreased sexual development due to hypogonadism, macroglossia (enlarged tongue), and enamel hypoplasia leading to increased caries susceptibility. These features are pathognomonic of trisomy 21. Other syndromes do not present with this specific constellation of findings.
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Large anterior fontanelles, open structure, slanting eyes, decreased sexual development, macroglossia and enamel hypoplasia are seen in 1. Carniofacial dysostosis 2. Down"s syndrome 3. Treacher Collins syndrome 4. Marfan"s syndrome
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#6Oral Pathology
Agranulocytosis may resemble necrotizing ulcerative gingivitis.
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Agranulocytosis may involve early lesions of the oral mucosa and the gingiva that are non-spcific but resemble 1. Erythematous stomatitis 2. Acute herpetic stomatitis 3. Necrotizing ulcerating gingivitis 4. Non specific vesiculobullous stomatitis
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#7Oral Pathology
White sponge nevus is a hereditary condition presenting with bilateral, pearly white, soft, thickened areas of buccal mucosa present since birth. The familial history (younger brother also affected) and congenital nature are characteristic. Leukoedema is acquired and disappears with stretching, lichen planus is typically acquired in adults, and mucous patches are related to secondary syphilis.
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A young patient has bilateral, pearly white thickening of the buccal mucosa since birth. His younger brother also has similar lesions. History and clinical findings are consistent with a diagnosis of 1. Leukoedema 2. White sponge nevus 3. Lichen planus 4. Mucous patches
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#8Oral Pathology
Crest syndrome is a variant of hidebound disease.
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One variant of hidebound disease is which syndrome? 1. Down"s syndrome 2. Crest syndrome 3. Greenspan"s syndrome 4. Kleinfelter"s syndrome
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#9Oral Pathology
Epiphora (excessive tearing) is an associated symptom of periodic migrainous neuralgia (cluster headache). Cluster headaches are accompanied by autonomic symptoms including lacrimation, nasal congestion, and conjunctival injection on the affected side. Trigeminal neuralgia, acute periodontitis, and ptyalism are not typically associated with excessive tearing.
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Epiphora is one of the associated symptoms in 1. Trigeminal neuralgia 2. Acute periodontitis 3. Periodoic migrainous neuralgia 4. Ptyalism
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