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Lint: 1p36-deletion-syndrome

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

"Clinical features"

Line 4:1 · "Clinical features" is not a recognised heading for this article type.
There Is
suggestion

"There is a broad spectrum of variability in the clinical presentation of monosomy 1p36. Some of the neurodevelopmental and physical abnormalities that may be present in 1p36 deletion syndrome are featured below 1,3:"

Line 5:4 · Don't start a sentence with 'There is'.
Commas
suggestion

"Findings on antenatal ultrasound, such as ventriculomegaly, cardiac malformations, and midface hypoplasia, sometimes associated with intrauterine growth restriction (IUGR), as well as various other anomalies, should prompt suspicion for 1p36 deletion syndrome 5."

Line 53:36 · More than 5 commas in a single sentence might make it more difficult to read.