Nokea
Which is the most common causative agent of bacterial endocarditis?
- A. Staphylococcus albus
- B. Streptococcus hemolyticus
- C. Staphylococcus albicans
- D. Streptococcus viridans
Correct Answer: D
Rationale: S. viridans is the most common causative agent in bacterial (infective) endocarditis.
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Proteins found in muscle fibres include:
- A. Vimentin
- B. Saccharin
- C. Keratin
- D. Desmin
Correct Answer: D
Rationale: Desmin: Desmin is an intermediate filament protein found in muscle fibers, playing a critical role in maintaining structural integrity and organization within muscle cells.
The most common cause for testicular pain in boys in 2-10 years of age is
- A. Testicular torsion
- B. Torsion of appendix testis
- C. Epididymitis
- D. Congenital varicocele
Correct Answer: B
Rationale: Torsion of the appendix testis is the most common cause of testicular pain in boys aged 2-10 years, as it involves the twisting of a small vestigial remnant.
The most appropriate first-line treatment for status epilepticus in a child is:
- A. Diazepam
- B. Phenytoin
- C. Carbamazepine
- D. Valproate
Correct Answer: A
Rationale: Diazepam is commonly used as the first-line treatment in managing status epilepticus due to its fast-acting, long-lasting anticonvulsant effects.
Features predisposing to NEC (necrotising enterocolitis) in the neonatal period include:
- A. Short fixation
- B. Asphyxia
- C. Umbilical artery catheter
- D. Maternal Crohn's disease
Correct Answer: B
Rationale: Asphyxia is a known risk factor for necrotizing enterocolitis (NEC) due to its effect on intestinal blood flow, leading to bowel ischemia and increased risk of bacterial translocation.
The following are transmitted as autosomal dominant traits:
- A. Congenital spherocytosis
- B. Vitamin D-resistant rickets
- C. CAH
- D. Hereditary haemorrhagic telangiectasia
Correct Answer: D
Rationale: Hereditary haemorrhagic telangiectasia is an autosomal dominant disorder. Congenital spherocytosis and Vitamin D-resistant rickets can also be autosomal dominant, but CAH (Congenital Adrenal Hyperplasia) is typically autosomal recessive.