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Lint: beckwith-wiedemann-syndrome-2

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

"Associations"

Line 22:1 · "Associations" is under the wrong parent heading (found under "Pathology").
There Is
suggestion

"The incidence is estimated at around 1:10,000 live births. As such, it is the most common overgrowth and cancer predisposition disorder 8,9. There is no gender or ethnicity predilection."

Line 19:156 · Don't start a sentence with 'There is'.
Biographical Lifespan
suggestion

"History and etymology"

Line 68:1 · A bold element in the History and etymology section should be a person; it would be useful to have their lifespan details: '<h4>History and etymology</h4> <p>First described independently by <strong>J B Beckwith</strong> '
Semicolons
suggestion

"Perlman syndrome: extremely rare; organomegaly, nephroblastomatosis, unique facial features, predisposition to developing Wilms tumour"

Line 73:47 · Use semicolons judiciously.

"Simpson-Golabi-Behmel syndrome: X-linked recessive inheritance; hypertelorism, macrocephaly, macrostomia, coarse features, intellectual disability"

Line 74:77 · Use semicolons judiciously.

"Sotos syndrome: autosomal dominant with sporadic mutations; advanced bone age, acromegaly, macrocephaly, dolichocephaly, frontal bossing, downward slanting palpebral fissures, prognathism (protruding mandible), pointed chin, intellectual disability"

Line 75:73 · Use semicolons judiciously.

"Weaver syndrome: extremely rare, autosomal dominant; frontal bossing, round face, hypertelorism, micrognathia"

Line 76:66 · Use semicolons judiciously.
Commas
suggestion

"Sotos syndrome: autosomal dominant with sporadic mutations; advanced bone age, acromegaly, macrocephaly, dolichocephaly, frontal bossing, downward slanting palpebral fissures, prognathism (protruding mandible), pointed chin, intellectual disability"

Line 75:99 · More than 5 commas in a single sentence might make it more difficult to read.