PARTIAL TRISOMY DUE TO A DE NOVO DUPLICATION 22q11.1-22q13.1: A CAT-EYE SYNDROME VARIANT WITH BRAIN ANOMALIES

Karcaaltincaba D., Ceylaner S., Ceylaner G., Dalkilic S., Karli-Oguz K., Kandemir O.

GENETIC COUNSELING, cilt.21, sa.1, ss.19-24, 2010 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 21 Sayı: 1
  • Basım Tarihi: 2010
  • Dergi Adı: GENETIC COUNSELING
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.19-24
  • Hacettepe Üniversitesi Adresli: Evet

Özet

Partial trisomy due to a de novo duplication 22q11.1-22q13.1: a cat-eye syndrome variant with brain anomalies: We report a case of partial trisomy 22q with de nova duplication of chromosomal region 22q11.1-22q13.1, also confirmed by microarray comparative genomic hybridization (Array-CGH) analysis. The fetus had interhemispheric cyst and corpus callosum agenesis diagnosed by MRI which has not been reported in the literature. This novel phenotype differs from the reported cat eye syndromes by the absence of heart defects and the presence of brain anomalies.