Pregled bibliografske jedinice broj: 174078
Detection of De Novo Partial Trisomy 22qter
Detection of De Novo Partial Trisomy 22qter // European Journal of Human Genetics, 12 (2004), 1. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
CROSBI ID: 174078 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Detection of De Novo Partial Trisomy 22qter
Autori
Lasan Trčić, Ružica ; Letica, Ljiljana ; Tonković Đurišević, Ivana ; Crkvenac Gornik, Kristina ; Mužinić, Dubravka ; Begović, Davor
Izvornik
European Journal of Human Genetics (1018-4813) 12
(2004), 1;
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, kongresno priopcenje, znanstveni
Ključne riječi
De novo partial trisomy 22qter; FISH
Sažetak
Characterization of a small chromosomal segment by means of conventional cytogenetics, even when high resolution banding is applied, can be inconclusive. The identification of the origin of duplicated chromosomal material on 22p, otherwise very difficult to characterize, is offered as an example. It was done using the FISH. The analysis of peripheral lymphocytes from the propositus by means of conventional cytogenetics with standard resolution, was normal. The FISH with cosmid N85A3, which normally hybridizes to the terminal region of the chromosome 22 long arm, revealed 3 signals, two of which corresponded to the normal position, and one was found on the short arm of the derivate chromosome 22. The causes of the distal chromosome segment duplication often lead to the familial pericentric inversion, parents with the same probe having normal signals on the terminal position of the chromosome 22 long arm. Segmental aneusomy was not detected at original cytogenetic diagnosis because the extra material on the chromosome 22 short arm was compatible with polymorphism of the satellite region of 22p. Clinical features of this 3-year-old boy with a rare de novo chromosomal aberration was growth retardation at birth, mental and developmental retardation, including a smaller mandible, genital hypospadia, testicular retention, ventricular and pulmonary stenosis. The authors suggest a possible association of the patient’ s clinical features with the duplicated material at the distal part of chromosome 22 long arm.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
0108027
Ustanove:
Medicinski fakultet, Zagreb
Profili:
Ružica Lasan Trčić
(autor)
Ivana Tonković Đurišević
(autor)
Dubravka Mužinić-Belinec
(autor)
Davor Begović
(autor)
Ljiljana Letica
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE