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• W2801968868 abstract "We present the characterization of a case with a small supernumerary marker chromosome (sSMC) detected prenatally derived from Xq28 and 14q11.2 maternal translocation. A 33-year-old Japanese woman, primigravida, underwent amniocentesis because of fetal growth restriction and fetal structural abnormality at 30 weeks of gestation. The fetal karyotype was identified as 47,XY,+mar. Additionally, the single nucleotide polymorphism array analysis revealed copy number gains at Xq28 and 14q11.2. A male infant, weighing 1,391 g, was delivered at term by cesarean section. Maternal and paternal karyotypes were 46,X,t(X; 14)(q28; q11) and 46,XY, respectively. These findings indicated that the sSMC might have originated from chromosome disjunction at a ratio of three to one. Here we describe a case with an sSMC derived from Xq28 and 14q11.2. Our findings suggest that this sSMC is most likely pathogenic. The collection of additional cases may be required." @default.
• W2801968868 created "2018-05-17" @default.
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• W2801968868 date "2018-01-01" @default.
• W2801968868 modified "2023-09-24" @default.
• W2801968868 title "Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally" @default.
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• W2801968868 doi "https://doi.org/10.1155/2018/2875241" @default.
• W2801968868 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5964436" @default.
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