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Article Dans Anglais | IMSEAR | ID: sea-139750

Résumé

Inflammation of oral mucosa induced by anti neoplastic drugs is an important, dose limiting and costly side effect of cancer therapy. Here is presented an exacerbated case of oral mucositis associated with renal failure in a patient who underwent bone marrow transplantation. The clinical aspects and an integrated rehabilitation program are discussed below.


Sujets)
Protocoles de polychimiothérapie antinéoplasique/effets indésirables , Transplantation de moelle osseuse , Soins dentaires pour malades chroniques/méthodes , Femelle , Humains , Thérapie laser , Adulte d'âge moyen , Myélome multiple/complications , Myélome multiple/thérapie , Insuffisance rénale/complications , Stomatite/étiologie , Stomatite/thérapie , Conditionnement pour greffe/effets indésirables , Résultat thérapeutique
2.
Braz. j. med. biol. res ; 39(4): 555-561, Apr. 2006. ilus, tab
Article Dans Anglais | LILACS | ID: lil-425077

Résumé

The objective of the present study was to determine the frequency of somatic chromosomal anomalies and Y chromosomal microdeletions (azoospermia factor genes, AZF) in infertile males who seek assisted reproduction. These studies are very important because the assisted reproduction techniques (mainly intracytoplasmic sperm injection) bypass the natural selection process and some classical chromosomal abnormalities, microdeletions of AZF genes or some deleterious genic mutations could pass through generations. These genetic abnormalities can cause in the offspring of these patients male infertility, ambiguous external genitalia, mental retardation, and other birth defects. We studied 165 infertile men whose infertility was attributable to testicular problems (60 were azoospermic, 100 were oligospermic and 5 were asthenospermic). We studied 100 metaphases per patient with GTG banding obtained from temporary lymphocyte culture for chromosomal abnormality detection and performed a genomic DNA analysis using 28 Y chromosome-specific sequence-tagged sites for Y AZF microdeletion detection. Karyotyping revealed somatic anomalies in 16 subjects (16/165 = 9.6 percent). Of these 16, 12 were in the azoospermic group (12/60 = 20 percent) and 4 were in the oligospermic group (4/100 = 4 percent). The most common chromosomal anomaly was Klinefelter syndrome (10/165 = 6 percent). Microdeletions of AZF genes were detected in 12 subjects (12/160 = 7.5 percent). The frequencies detected are similar to those described previously. These results show the importance of genetic evaluation of infertile males prior to assisted reproduction. Such evaluation can lead to genetic counseling and, consequently, to primary and secondary prevention of mental retardation and birth defects.


Sujets)
Humains , Mâle , Délétion de segment de chromosome , Chromosomes Y humains/génétique , Délétion de gène , Infertilité masculine/génétique , Caryotypage , Oligospermie/génétique , Réaction de polymérisation en chaîne
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