Genomic imbalances associated with mullerian aplasia
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2008
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Resumo |
Background: Aplasia of the mullerian ducts leads to absence of the uterine corpus, uterine cervix, and upper (superior) vagina. Patients with mullerian aplasia (MA) often exhibit additional clinical features such as renal, vertebral and cardiac defects. A number of different syndromes have been associated with MA, and in most cases its aetiology remains poorly understood. Objective and methods: 14 syndromic patients with MA and 46, XX G-banded karyotype were screened for DNA copy number changes by similar to 1 Mb whole genome bacterial artificial chromosome (BAC) array based comparative genomic hybridisation (CGH). The detected alterations were validated by an independent method and further mapped by high resolution oligo-arrays. Results: Submicroscopic genomic imbalances affecting the 1q21.1, 17q12, 22q11.21, and Xq21.31 chromosome regions were detected in four probands. Presence of the alterations in the normal mother of one patient suggests incomplete penetrance and/or variable expressivity. Conclusion: 4 of the 14 patients (29%) were found to have cryptic genomic alterations. The imbalances on 22q11.21 support recent findings by us and others that alterations in this chromosome region may result in impairment of mullerian duct development. The remaining imbalances indicate involvement of previously unknown chromosome regions in MA, and point specifically to LHX1 and KLHL4 as candidate genes. |
Identificador |
JOURNAL OF MEDICAL GENETICS, v.45, n.4, p.228-232, 2008 0022-2593 http://producao.usp.br/handle/BDPI/27711 10.1136/jmg.2007.051839 |
Idioma(s) |
eng |
Publicador |
B M J PUBLISHING GROUP |
Relação |
Journal of Medical Genetics |
Direitos |
restrictedAccess Copyright B M J PUBLISHING GROUP |
Palavras-Chave | #ABSENT RADIUS SYNDROME #KUSTER-HAUSER-SYNDROME #HYBRIDIZATION #GENES #Genetics & Heredity |
Tipo |
article original article publishedVersion |