Radiopaedia Helpers

shprintzen-syndrome

Medical Misspellings

error

"persistent cavum septi pellucidi and/or cavum vergae (19-33%)"

Line 61:28 · This is a misspelling: use 'septa' rather than 'septi'.

List Caps

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"Mondini malformation"

Line 42:11 · In general, we don't start a list item with a capital letter. Exceptions are proper nouns.

Headings Valid

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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 40:1 · "Associations" is under the wrong parent heading (found under "Pathology").

There Is

suggestion

"There is a near-universal association with a deletion within chromosome 22q11.2. The majority of cases have de novo mutations. 22q11 deletions are associated with some types of conotruncal cardiac defects as well as conotruncal anomaly face syndrome ⁵."

Line 39:4 · Don't start a sentence with 'There is'.

Links

manifestations-of-22q112-deletion-syndrome-mnemonic