Tetrasomy 9p | |
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Other names | Isochromosome 9p |
Chromosome 9, the chromosome involved in this condition |
Tetrasomy 9p (also known tetrasomy 9p syndrome) is a rare chromosomal disorder characterized by the presence of two extra copies of the short arm of chromosome 9 (called the p arm), in addition to the usual two.[1] Symptoms of tetrasomy 9p vary widely among affected individuals but typically include varying degrees of delayed growth, abnormal facial features and intellectual disability.[1] Symptoms of the disorder are comparable to those of trisomy 9p.[2]