Partial Trisomy 1q41-qter and Partial Trisomy 9pter-9q21.32 in a Newborn Infant: An Array CGH Analysis and Review
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Wiley-Blackwell
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
We report on a girl who presented with distinctive abducted hip and hyperextended knee. Cytogenetic analysis detected an extra derivative chromosome resulting from a balanced translocation in the mother and 3:1 segregation. Using array comparative genomic hybridization (CGH) in combination with conventional high resolution GTG banding, we designate the karyotype as 47, XX, +der(9)t(1;9)(q41;q21.32)mat, indicating tertiary trisomy of chromosome segments 1q41-qter and 9pter-9q21.32. A review and genotype-phenotype correlation suggested that the patient represented most of the manifestations of duplication of chromosome arms 1q and 9p. To our knowledge, a similar case has so far not been reported. (c) 2013 Wiley Periodicals, Inc.
Açıklama
Anahtar Kelimeler
t(1, 9), duplication 1q41, duplication 9p, partial trisomy, array CGH
Kaynak
American Journal of Medical Genetics Part A
WoS Q Değeri
Scopus Q Değeri
Cilt
164
Sayı
2










