“… 7 Situs inversus can occur as an isolated condition or as part of syndrome like Kartagener’s syndrome associated with other abnormalities. 8 Kartgaener’s syndrome is known to occur as a triad of situs inversus, bronchiectasis and sinusitis and is also known as primary ciliary dyskinesia. 9 Our patient was not investigated for any genetic disorders as she was asymptomatic with regards to her situs condition.…”
Situs inversus is an uncommon condition in which there is transposition of thoracic and abdominal structures. We report a case of situs inversus totalis detected incidentally in a 72-year-old female under investigation for haematuria. The imaging findings and role of imaging in this condition have been described in detail. This article emphasises the need for the clinicians to be aware of situs anomalies before planning surgical or radiological interventions in these patients.
“… 7 Situs inversus can occur as an isolated condition or as part of syndrome like Kartagener’s syndrome associated with other abnormalities. 8 Kartgaener’s syndrome is known to occur as a triad of situs inversus, bronchiectasis and sinusitis and is also known as primary ciliary dyskinesia. 9 Our patient was not investigated for any genetic disorders as she was asymptomatic with regards to her situs condition.…”
Situs inversus is an uncommon condition in which there is transposition of thoracic and abdominal structures. We report a case of situs inversus totalis detected incidentally in a 72-year-old female under investigation for haematuria. The imaging findings and role of imaging in this condition have been described in detail. This article emphasises the need for the clinicians to be aware of situs anomalies before planning surgical or radiological interventions in these patients.
Normal and polyposal nasal mucosa differ essentially in sialic acid presentation, while nasal polyps from patients with CF have a higher level of various lectin-reactive galactoside residues than nasal polyps from those without CF.
\s=b\We investigated respiratory mucosa cilia ultrastructure in patients homozygous for the gene for Kartagener's syndrome (KS) and patients apparently phenotypic for KS who had bronchiectasis and sinusitis but without situs inversus.
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