Termos psicopatológicos em bandas e músicas de rock and roll

OBJETIVO: Investigar o uso de termos psicopatológicos nos nomes de bandas de rock and roll e em suas músicas. MÉTODO: Termos psicopatológicos do glossário do DSM-IV foram digitados em português e inglês na página do YouTube. Bandas e músicas de rock and roll foram identificadas. O mesmo procedimento foi realizado, a título de comparação, com o glossário de termos neurológicos da CID-10. RESULTADOS: Foram encontrados nomes de bandas ou músicas referentes a 62 termos psiquiátricos e a 24 termos neurológicos. Os termos psiquiátricos foram mais frequentes, apresentando diferença estatisticamente significativa. Foram encontradas 60 bandas de rock com nomes inspirados na psiquiatria e na neurologia. Dessas, 44 bandas usavam nomes psiquiátricos e 16 bandas usavam termos neurológicos. Bandas e músicas de rock usam mais nomes psiquiátricos que neurológicos. Predominaram nas músicas nomes relacionados ao uso de substâncias. Ao se compararem nomes de bandas e canções brasileiras e estrangeiras, não se encontrou diferença estatisticamente significativa. CONCLUSÃO: Bandas de rock and roll usam com maior frequência termos psicopatológicos em seus nomes e em suas músicas. Bandas brasileiras apresentam resultados semelhantes.

Alternative genotyping method for the single nucleotide polymorphism A2959G (AF159246) of the bovine CAST gene

The objective of this work was to genotype the single nucleotide polymorphism (SNP) A2959G (AF159246) of bovine CAST gene by PCR-RFLP technique, and to report its use for the first time. For this, 147 Bos indicus and Bos taurus x Bos indicus animals were genotyped. The accuracy of the method was confirmed through the direct sequencing of PCR products of nine individuals. The lowest frequency of the meat tenderness favorable allele (A) in Bos indicus was confirmed. The use of PCR-RFLP for the genotyping of the bovine CAST gene SNP was shown to be robust and inexpensive, which will greatly facilitate its analysis by laboratories with basic structure.

Função de afilamento para Virola surinamensis (Roll.) Warb

Este estudo foi conduzido com o propósito de gerar equação de afilamento para Virola surinamensis (Roll.) Warb, que está entre as espécies mais exportadas pela indústria madeireira do estuário amazônico. Foram testados os modelos de Kozak (1969), Baldwin (1991), Demaerschalk (1972) e Garay (1979). Todos esses modelos estimaram o diâmetro comercial com precisão, porém os três primeiros resultaram em inconsistência ao estimar a altura comercial. O modelo de Garay foi selecionado e utilizado para gerar uma curva de cubagem para a espécie.

Complete mole in a dichorionic twin pregnancy after intracytoplasmic sperm injection

A dichorionic twin pregnancy with complete hydatidiform mole and coexistent fetus is a rare and challenging situation, whose pathogenesis has not been yet fully understood. We present a case of a 39-year-old woman who underwent intracytoplasmic sperm injection with two embryos transfer. The 12-week gestation ultrasound examination revealed normal fetus and placenta with features of hydatidiform mole, leading to pregnancy termination. Autopsy and histological examinations diagnosed a complete mole coexisting with a normal fetus, and the genetic analysis showed a diploid fetus with biparental genome and molar tissue with paternal diploidy. This case highlighted that complete molar pregnancies may still occur even though pregnancy is achieved after intracytoplasmic sperm injection. A review of the literature was performed by collecting data from the few similar reported cases and by commenting on the pathogenesis of this rare condition.

Do induced twin pregnancies influence the obstetric and neonatal results of multiple births born before 32 weeks? Comparison to spontaneous gestation

PURPOSE: To compare obstetric outcomes of induced preterm twin births (under 32 weeks gestation) with those spontaneously conceived. METHODS: Prospective study of twin pregnancies (25 induced and 157 spontaneously conceived) developed over a period of 16 years in a tertiary obstetric center. Demographic factors, obstetric complications, gestational age at delivery, mode of delivery, birth weight and immediate newborn outcome were compared. RESULTS: The analysis of obstetrical complications concerning urinary or other infections, hypertensive disorders of pregnancy, gestational diabetes, fetal malformations, intrauterine fetal death, intrauterine growth restriction and intrauterine discordant growth reveal no significant statistical differences between the two groups. First trimester bleeding was higher in the induced group (24 versus 8.3%, p=0.029). The cesarean delivery rate was 52.2% in spontaneous gestations and 64% in induced gestations. Gestational age at delivery, birth weight, Apgar scores at first and fifth minutes, admissions to Neonatal Intensive Care Unit and puerperal complications show no statistically significant differences between the two groups. These results were independent of chorionicity and induction method. CONCLUSION: The mode of conception did not influence obstetric and neonatal outcomes. Although induced pregnancies have higher risk of first trimester bleeding, significant differences were not observed regarding other obstetric and puerperal complications and neonatal results.

Griscelli syndrome-type 2 in twin siblings: case report and update on RAB27A human mutations and gene structure

Griscelli syndrome (GS) is a rare autosomal recessive disorder caused by mutation in the MYO5A (GS1, Elejalde), RAB27A (GS2) or MLPH (GS3) genes. Typical features of all three subtypes of this disease include pigmentary dilution of the hair and skin and silvery-gray hair. Whereas the GS3 phenotype is restricted to the pigmentation dysfunction, GS1 patients also show primary neurological impairment and GS2 patients have severe immunological deficiencies that lead to recurrent infections and hemophagocytic syndrome. We report here the diagnosis of GS2 in 3-year-old twin siblings, with silvery-gray hair, immunodeficiency, hepatosplenomegaly and secondary severe neurological symptoms that culminated in multiple organ failure and death. Light microscopy examination of the hair showed large, irregular clumps of pigments characteristic of GS. A homozygous nonsense mutation, C-T transition (c.550C>T), in the coding region of the RAB27A gene, which leads to a premature stop codon and prediction of a truncated protein (R184X), was found. In patient mononuclear cells, RAB27A mRNA levels were the same as in cells from the parents, but no protein was detected. In addition to the case report, we also present an updated summary on the exon/intron organization of the human RAB27A gene, a literature review of GS2 cases, and a complete list of the human mutations currently reported in this gene. Finally, we propose a flow chart to guide the early diagnosis of the GS subtypes and Chédiak-Higashi syndrome.