Cystic Fibrosis

Descripción

A short MCQ on cystic fibrosis
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Test por chris.kingsnorth, actualizado hace más de 1 año
chris.kingsnorth
Creado por chris.kingsnorth hace alrededor de 9 años
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Resumen del Recurso

Pregunta 1

Pregunta
How many children are affected by CF in the UK?
Respuesta
  • 1 in 25,000
  • 1 in 2500
  • 1 in 250
  • 1 in 250,000

Pregunta 2

Pregunta
How many people are carriers of CF in the UK?
Respuesta
  • 1 in 25
  • 1 in 250
  • 1 in 25,000
  • 1 in 250,000

Pregunta 3

Pregunta
Inheritance of CF is autosomal dominant
Respuesta
  • True
  • False

Pregunta 4

Pregunta
∆F508 is the most common CF mutation
Respuesta
  • True
  • False

Pregunta 5

Pregunta
The defective protein in CF is called:
Respuesta
  • CFTR
  • CTFR
  • CRTF

Pregunta 6

Pregunta
In the most common mutation of CFTR, the protein can escape the ER but once in the cell membrane dose not function properly
Respuesta
  • True
  • False

Pregunta 7

Pregunta
Positive Guthrie testing for CF is diagnostic of the condition
Respuesta
  • True
  • False

Pregunta 8

Pregunta
Low Na concentration in sweat on sweat test suggests CF
Respuesta
  • True
  • False

Pregunta 9

Pregunta
Growth of patients with CF is unaffected
Respuesta
  • True
  • False

Pregunta 10

Pregunta
Clinical features of CF are similar in all patients
Respuesta
  • True
  • False

Pregunta 11

Pregunta
Which of the following medications are not used in treatment of CF?
Respuesta
  • Bronchodilators (e.g. salmeterol)
  • Anticholinergics (e.g. ipratropium)
  • Antibiotics
  • Steroids
  • Mucolytics (e.g. DNase)
  • Beta-blockers

Pregunta 12

Pregunta
CFTR modulators are currently the mainstay of treatment for CF in the UK
Respuesta
  • True
  • False

Pregunta 13

Pregunta
Median survival in CF is currently estimated at:
Respuesta
  • 31 years
  • 41 years
  • 51 years
  • 61 years
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