Tetrasomy of the short arm of chromosome 9: Prenatal diagnosis and further delineation of the phenotype
Gerald Bradley Schaefer, David B. Domek, Mark Aloysuis Morgan, Razia S. Muneer, Sarah F. Johnson
Abstract
Gerald Bradley Schaefer, David B. Domek, Mark Aloysuis Morgan, Razia S. Muneer, Sarah F. Johnson
Abstract
A fetus with multiple malformations was identified by prenatal ultrasound investigation. Cordocentesis and fetal lymphocyte chromosome analysis demonstrated a model number of 47 chromosomes. The extra chromosome material was identified as an isochromosome of the entire short arm of chromosome 9 with no involvement of the heterochromatic region of the long arm [47,XY, + i(9p)]. This represents the first report of prenatal diagnosis of tetrasomy 9p. Further delineation of the phenotype is discussed.
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A fetus with multiple malformations was identified by prenatal ultrasound investigation. Cordocentesis and fetal lymphocyte chromosome analysis demonstrated a model number of 47 chromosomes. The extra chromosome material was identified as an isochromosome of the entire short arm of chromosome 9 with no involvement of the heterochromatic region of the long arm [47,XY, + i(9p)]. This represents the first report of prenatal diagnosis of tetrasomy 9p. Further delineation of the phenotype is discussed.
Key concepts: Tetrasomy, Phenotype, Genetics, Long arm, Chromosome, Prenatal diagnosis, Biology, Medicine