دورية أكاديمية

De Novo 13q13.3-21.31 deletion involving RB1 gene in a patient with hemangioendothelioma of the liver.

التفاصيل البيبلوغرافية
العنوان: De Novo 13q13.3-21.31 deletion involving RB1 gene in a patient with hemangioendothelioma of the liver.
المؤلفون: Rapini, Novella, Lidano, Roberta, Pietrosanti, Silvia, Vitiello, Giuseppina, Grimaldi, Chiara, Postorivo, Diana, Nardone, Anna Maria, Del Bufalo, Francesca, Brancati, Francesco, Bitti, Maria Luisa Manca
المصدر: Italian Journal of Pediatrics; 2014, Vol. 40 Issue 1, p1-10, 10p
مصطلحات موضوعية: HEMANGIOMAS, LIVER diseases, GENETIC mutation, DATA analysis software, DESCRIPTIVE statistics
مستخلص: Interstitial deletions of the long arm of chromosome 13 (13q) are related with variable phenotypes, according to the size and the location of the deleted region. The main clinical features are moderate/severe mental and growth retardation, cranio-facial dysmorphism, variable congenital defects and increased susceptibility to tumors. Here we report a 3-yearold girl carrying a de novo 13q13.3-21.32 interstitial deletion. She showed developmental delay, growth retardation and mild dysmorphism including curly hair, high forehead, short nose, thin upper lip and long philtrum. An abnormal mass was surgically removed from her liver resulting in a hemangioendothelioma. Array analysis allowed us to define a deleted region of about 27.87 Mb, which includes the RB1 gene. This is the first report of a 13q deletion associated with infantile hemangioendothelioma of the liver. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:17208424
DOI:10.1186/1824-7288-40-5