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Chromosome 1p deletion syndrome: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion. More detailed information about the symptoms, causes, and treatments of Chromosome 1p deletion syndrome is available below.
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Deletion of the short arm of chromosome 1. Common symptoms include mental deficiency, malformed ears, short neck, bulbous nose, heart defects, finger abnormalities, and small deeply set eyes but the phenotype varies with the breakpoint. - (Source - Diseases Database)
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