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Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion.
Kurtulgan, Hande Küçük; Özer, Leyla; Yildirim, Malik Ejder; Ünsal, Evrim; Aktuna, Süleyman; Baltaci, Volkan; Akkus, Nejmiye; Sezgin, Ilhan.
Affiliation
  • Kurtulgan HK; Cumhuriyet University School of Medicine Division of Medical Genetics, Sivas, Turkey.
  • Özer L; Mikrogen Genetic Diagnosis Center, Cinnah Street 47/1 Çankaya, Ankara, Turkey.
  • Yildirim ME; Cumhuriyet University School of Medicine Division of Medical Genetics, Sivas, Turkey.
  • Ünsal E; Division of Histology and Embryology, Yeni Yüzyil University School of Medicine, Istanbul, Turkey.
  • Aktuna S; Medicine Division of Medical Biology and Genetics, Yeni Yüzyil University School of Medicine, Istanbul, Turkey.
  • Baltaci V; Medicine Division of Medical Biology and Genetics, Yeni Yüzyil University School of Medicine, Istanbul, Turkey.
  • Akkus N; Cumhuriyet University School of Medicine Division of Medical Genetics, Sivas, Turkey.
  • Sezgin I; Cumhuriyet University School of Medicine Division of Medical Genetics, Sivas, Turkey.
Mol Cytogenet ; 8: 92, 2015.
Article in En | MEDLINE | ID: mdl-26594242
ABSTRACT

BACKGROUND:

14q duplications caused by parental pericentric inversion of chromosome 14 are rarely reported and no clear genotype-phenotype correlation has been determined yet. CASE PRESENTATION Here we reported a 7 years old female patient with recombinant chromosome characterized by 14 q duplication and originated from maternal pericentric inversion of chromosome 14. Principal clinical findings of the child include developmental delay, microcephaly, hypertelorism, low set ears, clinodactyly of fifth fingers, hypotonia, telecanthus and cardiac malformation.

CONCLUSIONS:

Her final karyotype was 46,XX,rec(14)dup(14q)inv(14)(p11.2q24)mat,arr14q24.1-qter(64,800,000-108,350,000 bp)x3.
Key words