Early recurrent left atrial myxoma in a teenager with de novo mutation of Carney complex.

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dc.contributor.authorStajevic, Mila S
dc.contributor.authorVukomanovic, Vladislav A
dc.contributor.authorKuburovic, Vladimir D
dc.contributor.authorDjuricic, Slavisa M
dc.date.accessioned2012-06-11T09:10:28Z
dc.date.available2012-06-11T09:10:28Z
dc.date.issued2011-05
dc.description.abstractWe report a case of an extremely early recurrence of left atrial myxoma in a 13-year-old girl. On hospital admission, the clinical presentation was of cerebral embolism with noticeable spotty skin pigmentation and hypertelorism. The left atrial myxoma originated from the roof of the left atrium. The histology specimen showed typical finding of a myxoma. Six months later a new intracardial mass was evacuated, the postoperative result showing the same type of myxomatous tissue. Genetic investigations demonstrated Carney complex. The genetic analysis of the child's family was negative, demonstrating de novo mutation of this rare disorder.en_US
dc.identifier.citationStajevic Mila S, Vukomanovic Vladislav A, Kuburovic Vladimir D, Djuricic Slavisa M. Early recurrent left atrial myxoma in a teenager with de novo mutation of Carney complex. Indian Journal of Human Genetics. 2011 May; 17(2): 108-110.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/138947
dc.language.isoenen_US
dc.source.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214313/en_US
dc.subjectCarneyen_US
dc.subjectleft atriumen_US
dc.subjectmyxomaen_US
dc.subjectrecurrenceen_US
dc.titleEarly recurrent left atrial myxoma in a teenager with de novo mutation of Carney complex.en_US
dc.typeArticleen_US
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