Class II Analphoid Chromosome in a Child with Aberrant Chromosome 7: A Rare Cytogenetic Association

2015 ◽  
Vol 146 (2) ◽  
pp. 120-123 ◽  
Author(s):  
Madhavan Jeevan Kumar ◽  
Rangasamy Ashok Kumar ◽  
Venugopal Subhashree ◽  
Thanikachalam Jayasudha ◽  
Venkatasubramanian Hemagowri ◽  
...  

A neocentromere is a functional centromere that has arisen within a region not known to have a centromere. We present a case with a very rarely reported class II neocentromere formation in an aberrant chromosome 7. A 22-month-old male was referred because of dysmorphic features. Banding cytogenetics was performed, and a ring 7 and a supernumerary marker chromosome along with a normal chromosome 7 were found. In situ hybridization using a centromeric probe revealed 46 signals, of which 2 signals for chromosome 7 were observed, one on the normal and one on the ring chromosome. Further analysis using FISH revealed that the linear acentric fragment was part of the 7q region, which suggests that there could be a possible McClintock mechanism.

1991 ◽  
Vol 96 (2) ◽  
pp. 203-210 ◽  
Author(s):  
Chris R. Schad ◽  
William J. Kraker ◽  
Syed M. Jalal ◽  
Martin S. Tallman ◽  
Harold N. Londer ◽  
...  

2013 ◽  
Vol 16 (1) ◽  
pp. 13-19 ◽  
Author(s):  
R.S. Guilherme ◽  
E Klein ◽  
A.B. Hamid ◽  
S Bhatt ◽  
M Volleth ◽  
...  

Abstract Twenty-nine as yet unreported ring chromosomes were characterized in detail by cytogenetic and molecular techniques. For FISH (fluorescence in situ hybridization) previously published high resolution approaches such as multicolor banding (MCB), subcentromere-specific multi-color-FISH (cenM-FISH) and two to three-color-FISH applying locus-specific probes were used. Overall, ring chromosome derived from chromosomes 4 (one case), 10 (one case), 13 (five cases), 14, (three cases), 18 (two cases), 21 (eight cases), 22 (three cases), X (five cases) and Y (one case) were studied. Eight cases were detected prenatally, eight due developmental delay and dysmorphic signs, and nine in connection with infertility and/or Turner syndrome. In general, this report together with data from the literature, supports the idea that ring chromosome patients fall into two groups: group one with (severe) clinical signs and symptoms due to the ring chromosome and group two with no obvious clinical problems apart from infertility.


2002 ◽  
Vol 33 (3) ◽  
pp. 279-284 ◽  
Author(s):  
Peter H. Wessels ◽  
Albert Twijnstra ◽  
Alfons G. H. Kessels ◽  
Bela Krijne-Kubat ◽  
Paul H. Theunissen ◽  
...  

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