RESUMEN
Mental retardation and hypotonia are found in virtually all Down syndrome (DS) individuals, whereas congenital heart defects (CHDs) are only present in a subset of cases. Although there have been numerous reports of the frequency of CHDs in DS, few of the studies have had complete ascertainment of DS in a defined geographic area. The Atlanta Down Syndrome Project, a population-based study of infants born with trisomy 21, provides such a resource. In the first 6.5 years of the study, 243 trisomy 21 livebirths were identified in the five-county Atlanta area (birth prevalence: 9.6/10,000). Cardiac diagnoses were available on 227 (93%) of the cases and 89% of these evaluations were made by echocardiography, cardiac catheterization, surgery, or autopsy. Of the 227 DS infants, 44% had CHDs including 45% atrioventricular septal defect (with or without other CHDs), 35% ventricular septal defect (with or without other CHDs), 8% isolated secundum atrial septal defect, 7%, isolated persistent patent ductus arteriosus, 4% isolated tetralogy of Fallot, and 1% other. This report is unique in that it contains the largest number of trisomy 21 infants ascertained in a population-based study where modern techniques for diagnosing cardiac abnormalities predominate.
Asunto(s)
Síndrome de Down/fisiopatología , Cardiopatías Congénitas , Humanos , Recién NacidoRESUMEN
Recent studies of trisomy 21 have shown that altered levels of recombination are associated with maternal non-disjunction occurring at both meiosis I (MI) and meiosis II (MII). To comprehend better the association of recombination with nondisjunction, an understanding of the pattern of meiotic exchange, i.e. the exchange of genetic material at the four-strand stage during prophase, is required. We examined this underlying exchange pattern to determine if specific meiotic configurations are associated with a higher risk of non-disjunction than others. We examined the crossover frequencies of chromosome 21 for three populations: (i) normal female meiotic events; (ii) meiotic events leading to MI non-disjunction; and (iii) those leading to MII non-disjunction. From these crossover frequencies, we estimated the array of meiotic tetrads that produced the observed crossovers. Using this approach, we found that nearly one-half of MI errors were estimated to be achiasmate. The majority of the remaining MI bivalents had exchanges that clustered at the telomere. In contrast, exchanges occurring among MII cases clustered at the pericentromeric region of the chromosome. Unlike the single exchange distributions, double exchanges from the non-disjoined populations seemed to approximate the distribution in the normal population. These data suggest that the location of certain exchanges makes a tetrad susceptible to non-disjunction. Specifically, this susceptibility is associated with the distance between the centromere and closest exchange. This result challenges the widely held concept that events occurring at MII are largely independent of events occurring at MI, and suggests that all non-disjunction events may be initiated during MI and simply resolved at either of the two meiotic stages.
Asunto(s)
Cromosomas Humanos Par 21/genética , Intercambio Genético , Síndrome de Down/genética , No Disyunción Genética , Femenino , Marcadores Genéticos , Humanos , Edad Materna , Meiosis/genética , Mitosis/genética , Profase/genética , TelómeroRESUMEN
Management of cardiogenic shock following neonatal myocardial infarction (MI) has received little attention in the literature. Advances in medical support have been pharmacologic in nature, yet the outcome remains dismal. We report the course of a neonate after MI. Extracorporeal membrane oxygenation was utilized for hemodynamic support during the immediate post-MI period. The patient initially was in massive cardiogenic shock, but her myocardial function recovered completely. She has a normal neurodevelopmental outcome at 22 months of age.
Asunto(s)
Infarto del Miocardio/terapia , Electrocardiografía , Oxigenación por Membrana Extracorpórea , Femenino , Humanos , Recién Nacido , Infarto del Miocardio/complicaciones , Choque Cardiogénico/etiologíaRESUMEN
The cause of non-disjunction of chromosome 21 remains largely unknown. Advanced maternal age is associated with both maternal meiosis I (MI) and meiosis II (MII) non-disjunction events. While reduced genetic recombination has been demonstrated in maternal MI errors, the basis for MII errors remains uncertain. We studied 133 trisomy 21 cases with maternal MII errors to test the hypothesis that segregation at MII may also be influenced by genetic recombination. Our data support a highly significant association: MII non-disjunction involves increased recombination that is largely restricted to proximal 21q. Thus, while absence of a proximal recombination appears to predispose to non-disjunction in MI, the presence of a proximal exchange predisposes to non-disjunction in MII. These findings profoundly affect our understanding of trisomy 21 as they suggest that virtually all maternal non-disjunction results from events occurring in meiosis I.
Asunto(s)
Cromosomas Humanos Par 21 , Síndrome de Down/genética , Meiosis/genética , No Disyunción Genética , Adulto , Síndrome de Down/embriología , Embrión de Mamíferos , Femenino , Feto , Humanos , Masculino , Edad Materna , Modelos Genéticos , Recombinación GenéticaAsunto(s)
Aneuploidia , Aberraciones Cromosómicas/epidemiología , Aberraciones Cromosómicas/etiología , Aborto Espontáneo/epidemiología , Trastornos de los Cromosomas , Femenino , Fertilización , Muerte Fetal , Humanos , Incidencia , Recién Nacido , Masculino , Edad Materna , Oocitos/fisiología , Embarazo , Recombinación Genética , Espermatozoides/fisiología , TrisomíaRESUMEN
Sucrose density centrifugation has been used to characterize the relative levels of AChE molecular forms in different parts of the brain, during development, or in various disease states. We have examined the influence of various tissue or sample storage and handling techniques on the abundance of the 4S and 10S molecular forms of AChE in rat forebrain. Our results demonstrate that freezing either a subcellular fraction or the intact tissue causes dramatic shifts in the level of the 4S and 10S molecular forms as compared to the values obtained in fresh tissue. Total AChE activity was unchanged suggesting that 4S and 10S forms are equally active and that 4S AChE is easily dissociated from 10S. These observations suggest that 4S and 10S molecular forms in brain are extremely labile and that great care should be taken when studying the factors that regulate these forms.