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Partial trisomy 4q and partial monosomy 9p in a girl with choanal atresia and various dysmorphic findings.
Cakmak-Genc, Gunes; Karakas-Celik, Sevim; Dursun, Ahmet; Piskin, Ibrahim Etem.
Afiliación
  • Cakmak-Genc G; Bulent Ecevit University, Faculty of Medicine, Department of Medical Genetics, Zonguldak, Turkey. Electronic address: gunes.cak@hotmail.com.
  • Karakas-Celik S; Bulent Ecevit University, Faculty of Medicine, Department of Medical Genetics, Zonguldak, Turkey.
  • Dursun A; Bulent Ecevit University, Faculty of Medicine, Department of Medical Genetics, Zonguldak, Turkey.
  • Piskin IE; Bulent Ecevit University, Faculty of Medicine, Department of Pediatrics, Zonguldak, Turkey.
Gene ; 568(2): 211-4, 2015 Sep 01.
Article en En | MEDLINE | ID: mdl-25979671
ABSTRACT
We report a new-born girl with partial trisomy of 4q28-qter and partial monosomy of 9p24-9ter. Our patient has choanal atresia, hypertelorism, wide nasal bridge, high arched palate, discrete nipples, heart defects, myoclonic seizures and various dysmorphic findings. Standard chromosomal analysis with G-banding with Trypsin-Giemsa revealed 46,XX,der(9)t(4;9)(q28;p24) resulting from the mother's t(4,9) (q28;p24) karyotype. Deletions of the terminal part of 9p and partial trisomy of chromosome 4q are rare chromosomal alterations. To our knowledge, this is the first report of choanal atresia in a patient with a partial trisomy of 4q28-qter and partial monosomy 9p24-9ter combination, which were detected by integrated cytogenetic and genomic analysis.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trisomía / Anomalías Múltiples / Atresia de las Coanas Tipo de estudio: Diagnostic_studies Límite: Female / Humans / Newborn Idioma: En Revista: Gene Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trisomía / Anomalías Múltiples / Atresia de las Coanas Tipo de estudio: Diagnostic_studies Límite: Female / Humans / Newborn Idioma: En Revista: Gene Año: 2015 Tipo del documento: Article
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