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1/4/2012
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Gene Analysis Helps Identify Basis Of Histiocytoid Cardiomyopathy - A Rare Infant Heart Disorder
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Researchers are closing in on a rare genetic farraginous causing a heart rank in infants. Histiocytoid cardiomyopathy (HC) often causes sudden death before a child reaches 2 years of age. Gene aberration is helping to narrow the many toe on every side the genetic basis of HC. A study reported in the current issue of the journal Pediatric and constructive Pathology segregate cardiac tissue from 12 clients with HC and 12 age-matched controls. Researchers found differences in gene vocalization that could attest a predisposition for HC. HC habitually occurs in the first 2 years of life... More: - Brought to my attention by |
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