A Case with de novo t (4;22) in Addition to Maternal inv 9

AYŞEGÜL ZAMANİ, HATİCE GÜL DURSUN, RUHUŞEN KUTLU

  • Yıl : 2001
  • Cilt : 17
  • Sayı : 4
  •  Sayfa : 243-246
A 8- mounth- old gir! was referred to our laboratory because of Down Syndrome. She had had phenotypical features as mild mental retardation, flated nasal bridge, low- set and malformed ears. İn detailed family history, her mother had had an carbon monoxide poisoning during proband’s pregnancy and an abortus before her. Chromosome analysis was carried on peripheral blood lymphocytes culture, using standart technigues and chromosomes were identified by using GTG, C and NOR- banding. Her karyotype was foundjo be 46, XX, t (4q;22q), inv(9). Family studies were shovved that neither her mother nor her father had carried this translocation but inv(9) was inherited from her mother to our patient. Our patient who seems as though a de novo balanced translocation carrier was discussed under the light of literatüre with her biochemical, radiologic and clinic features.
Atıf yapmak için :
Açıklama : Yazarların hiçbiri, bu makalede bahsedilen herhangi bir ürün, aygıt veya ilaç ile ilgili maddi çıkar ilişkisine sahip değildir. Araştırma, herhangi bir dış organizasyon tarafından desteklenmedi.Yazarlar çalışmanın birincil verilerine tam erişim izni vermek ve derginin talep ettiği takdirde verileri incelemesine izin vermeyi kabul etmektedirler.
A Case with de novo t (4;22) in Addition to Maternal inv 9
, Vol. 17 (4)
Geliş Tarihi : 17.01.2001, Kabul Tarihi : 17.01.2001, Yayın Tarihi : 02.10.2020
Selçuk Tıp Dergisi
ISSN:1017-6616;
E-ISSN:2149-8059;