Login
Toggle sidebar

Lint: dicer1-syndrome-1

dicer1-syndrome-1
Emphasis
warning

"DICER1 syndrome results from heterozygous germline loss-of-function mutation of the tumour suppressor gene DICER1 that encodes the endoribonuclease protein Dicer 1-5,8."

Line 33:111 · Italics should be used only in exceptional circumstances: '<em>DICER1</em>'
Headings Valid
warning

Expected headings

  • H1 Terminology
  • H1 Usage
  • H1 Epidemiology
  • H2 Risk factors
  • H2 Associations
  • H1 Clinical presentation
  • H2 Complications
  • H1 Diagnosis
  • H2 Diagnostic criteria
  • H2 Diagnostic clues
  • H1 Pathology
  • H2 Aetiology
  • H2 Location
  • H2 Classification
  • H2 Macroscopic appearance
  • H2 Microscopic appearance
  • H2 Immunophenotype
  • H2 Markers
  • H2 Genetics
  • H1 Radiographic features
  • H2 Plain radiograph
  • H2 Mammography
  • H2 Antenatal ultrasound
  • H2 Transoesophageal echocardiography
  • H2 Ultrasound
  • H2 CT
  • H3 Dual-energy CT
  • H2 Angiography (DSA)
  • H2 MRI
  • H2 CT/MRI
  • H2 Nuclear medicine
  • H3 PET-CT
  • H3 PET-MRI
  • H1 Radiology report
  • H1 Treatment and prognosis
  • H2 Complications
  • H1 History and etymology
  • H1 Differential diagnosis
  • H2 Clinical differential diagnosis
  • H1 Practical points
  • H1 See also

""

Line 34:1 · "" is not a recognised heading for this article type.
Oxford Comma
suggestion

"DICER1 syndrome most commonly manifests in children, adolescents and young adults 8."

Line 3:47 · Use the Oxford comma in 'children, adolescents and young'.
Links
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
6
4
0
0
0