Weidenbach, M <br/><br/>
Acute mitral regurgitation due to chordal rupture in a patient with neonatal Marfan syndrome caused by a deletion in exon 29 of the FBN1 gene.  [electronic resource] 

 -  Pediatric cardiology   
 - 382-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0172-0643 
<br/><br/><label>Standard No.: </label>10.1007/s002469900493  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acute Disease<br/>Cause of Death<br/>Chordae Tendineae<br/>DNA Mutational Analysis<br/>Echocardiography, Doppler, Color<br/>Exons--genetics<br/>Fatal Outcome<br/>Fibrillin-1<br/>Fibrillins<br/>Gene Deletion<br/>Heart Diseases--genetics<br/>Heart Failure--genetics<br/>Humans<br/>Infant<br/>Marfan Syndrome--complications<br/>Microfilament Proteins--genetics<br/>Mitral Valve Insufficiency--diagnostic imaging<br/>Rupture, Spontaneous