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1.
Genet. mol. biol ; 34(4): 557-561, 2011. ilus
Artigo em Inglês | LILACS | ID: lil-605945

RESUMO

The Peutz-Jeghers syndrome (PJS) is an autosomal-dominant hamartomatous polyposis syndrome characterized by mucocutaneous pigmentation, gastrointestinal polyps and the increased risk of multiple cancers. The causative point mutation in the STK11 gene of most patients accounts for about 30 percent of the cases of partial and complete gene deletion. This is a report on a girl with PJS features, learning difficulties, dysmorphic features and cardiac malformation, bearing a de novo 1.1 Mb deletion at 19p13.3. This deletion encompasses at least 47 genes, including STK11. This is the first report on 19p13.3 deletion associated with a PJS phenotype, as well as other atypical manifestations, thereby implying a new contiguous gene syndrome.


Assuntos
Humanos , Feminino , Adolescente , Cromossomos Humanos Par 19/genética , Síndrome de Peutz-Jeghers/genética , Proteínas Serina-Treonina Quinases/genética , Aberrações Cromossômicas , Deleção Cromossômica , Hibridização Genômica Comparativa , Mapeamento de Sequências Contíguas
2.
J. appl. oral sci ; 18(2): 166-170, Mar.-Apr. 2010. ilus, tab
Artigo em Inglês | LILACS | ID: lil-550408

RESUMO

OBJECTIVE: The present study evaluated the association between lactotransferrin (LTF) gene polymorphism (exon 2, A/G, Lys/Arg) and dental caries. MATERIAL AND METHODS: A convenience sample of 110 individuals, 12 years old, was divided into: group 1, 48 individuals without caries experience (DMFT=0), and group 2, 62 subjects with caries experience (DMFT>1). DNA was obtained from a mouthwash with 3 percent glucose solution, followed by a scrapping of the oral mucosa. After DNA purification, polymerase chain reaction (PCR), single strand conformation polymorphism (SSCP) was performed to access the study polymorphism. The LTF A/G (Lys/Arg) polymorphism had been previously reported as located in exon 1. RESULTS: Allele 1 of the study polymorphism was associated with low DMFT index and showed a protective effect against caries experience (OR=0.16, IC=0.03-0.76, p=0.01). CONCLUSIONS: Lactotransferrin A/G (exon 2, Lys/Arg) polymorphism was associated with susceptibility to dental caries in 12-year-old students.


Assuntos
Criança , Humanos , Suscetibilidade à Cárie Dentária/genética , Cárie Dentária/genética , Lactoferrina/genética , Alelos , Substituição de Aminoácidos , Arginina , Sequência de Bases , Estudos de Casos e Controles , Índice CPO , Análise Mutacional de DNA , Frequência do Gene , Lisina , Dados de Sequência Molecular , Polimorfismo de Nucleotídeo Único , Polimorfismo Conformacional de Fita Simples , Saliva
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