Document Detail


Chromosomal abnormalities as a cause of recurrent abortions in Egypt.
MedLine Citation:
PMID:  22090718     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: In 4%-8% of couples with recurrent abortion, at least one of the partners has chromosomal abnormality. Most spontaneous miscarriages which happen in the first and second trimesters are caused by chromosomal abnormalities. These chromosomal abnormalities may be either numerical or structural.
MATERIAL AND METHODS: Cytogenetic study was done for 73 Egyptian couples who presented with recurrent abortion at Genetic Unit of Children Hospital, Mansoura University.
RESULTS: We found that the frequency of chromosomal abnormalities was not significantly different from that reported worldwide. Chromosomal abnormalities were detected in 9 (6.1%) of 73 couples. Seven of chromosomal abnormalities were structural and two of them were numerical.
CONCLUSION: Our results showed that 6.1% of the couples with recurrent abortion had chromosomal abnormalities, with no other abnormalities. We suggest that it is necessary to perform cytogenetic in vestigation for couples who have recurrent abortion.
Authors:
Faeza Abdel Mogib El-Dahtory
Related Documents :
7919658 - Msx1 is close but not allelic to either hm or hx on mouse chromosome 5.
16620218 - Keratin 17 mutation in pachyonychia congenita type 2 patient with early onset steatocys...
23615628 - Microrna-323-3p: a new biomarker and potential therapeutic target for rheumatoid arthri...
17709468 - Growth and drug resistance phenotypes resulting from cytomegalovirus dna polymerase reg...
9045828 - The diviva minicell locus of bacillus subtilis.
3193098 - Cytogenetic evidence for two species within the current concept of the malaria vector a...
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Indian journal of human genetics     Volume:  17     ISSN:  0971-6866     ISO Abbreviation:  Indian J Hum Genet     Publication Date:  2011 May 
Date Detail:
Created Date:  2011-11-17     Completed Date:  2011-11-23     Revised Date:  2013-05-29    
Medline Journal Info:
Nlm Unique ID:  101223637     Medline TA:  Indian J Hum Genet     Country:  India    
Other Details:
Languages:  eng     Pagination:  82-4     Citation Subset:  -    
Affiliation:
Department of Genetics Unit of Children Hospital, Mansoura University, Mansoura, Egypt.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Cytoprotective effect of honey against chromosomal breakage in fanconi anemia patients in vitro.
Next Document:  Association of cytotoxic T lymphocyte-associated antigen 4 gene single nucleotide polymorphism with ...