Síndrome de Kartagener, reporte de caso
Introduction: Kartagener Syndrome is a clinical variant of primary ciliary dyskinesia It is a rare autosomal recessive disease, one in every 32,000 births, characterized by a triad of bronchiectasis, chronic sinusitis and situs inversus partial o total. We present the case...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | Spanish |
| Published: |
Colegio Médico de Honduras
2024-12-01
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| Series: | Revista Médica Hondureña |
| Subjects: | |
| Online Access: | https://www.camjol.info/index.php/RMH/article/view/18813 |