Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 11 de 11
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Am J Perinatol ; 7(2): 160-5, 1990 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-2331279

RESUMO

We reviewed the perinatal management and subsequent outcome of infants 401 to 800 gm birthweight delivered in 1983 to 1985 compared with those born in 1980 to 1982. Intrapartum fetal heart rate monitoring, cesarean section delivery, attempted delivery room resuscitation, and 5-minute Apgar scores greater than 5 were more frequent in 1983 to 1985. Significantly greater neonatal survival was evident for infants 500 to 700 gm birthweight (31%) and 24 to 27 weeks' gestation (45%) in 1983 to 1985, p less than 0.005. Infant birthweight, gestational age, gender, and 5-minute Apgar score, in addition to intrapartum tocolysis use, were predictors of higher survival by stepwise discriminant analysis. At a mean follow-up of 27 months, 13% (6 of 46) born in 1983 to 1985 had major disability compared with 67% (6 of 9) of infants born in 1980 to 1982. There has been a significant increase in survival and improvement in neurodevelopmental follow-up status for infants less than 801 gm birthweight. These improved outcome data should be considered by caregivers providing perinatal management and counseling parents regarding extremely low birthweight infants.


Assuntos
Mortalidade Infantil , Malformações do Sistema Nervoso , Resultado da Gravidez/epidemiologia , Índice de Apgar , Peso ao Nascer , Feminino , Idade Gestacional , Frequência Cardíaca Fetal , Humanos , Recém-Nascido de Baixo Peso , Recém-Nascido , Gravidez , Cuidado Pré-Natal , Tocólise
2.
Am J Med Genet ; 34(2): 268-70, 1989 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-2817010

RESUMO

We report on a case of synophthalmic cyclopia and alobar holoprosencephaly associated with an interstitial deletion of the short arm of chromosome 2: del(2)(p21p23). This is the second case with this phenotype in association with deletion in this region, and comparison with the infrequent other cases of 2p deletions suggests a causal relationship between band 2p21 and cyclopia.


Assuntos
Anormalidades Múltiplas/diagnóstico , Encéfalo/anormalidades , Deleção Cromossômica , Cromossomos Humanos Par 2 , Adulto , Cromossomos Humanos Par 13 , Cromossomos Humanos Par 18 , Ossos Faciais/anormalidades , Feminino , Morte Fetal , Humanos , Cariotipagem , Masculino , Gravidez , Diagnóstico Pré-Natal , Síndrome , Trissomia
3.
Proc Natl Acad Sci U S A ; 86(3): 1013-7, 1989 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-2521732

RESUMO

A cDNA clone encoding a human receptor for the Fc portion of IgG (Fc gamma R), Fc gamma RIII or CD16, was isolated from a human leukocyte library by a transient expression-immunoselection procedure. This cDNA (pGP5) encodes a 46-kDa phosphatidylinositol-linked cell surface protein with CD16 determinants and affinity for human IgG. The deduced protein sequence is most homologous to the murine receptor Fc gamma RII alpha, with slightly less homology to the human receptors Fc gamma RII and Fc epsilon RI. The cDNA hybridizes to a 2.2 kilobase mRNA in human leukocytes and a cloned human natural killer cell line. Fc gamma RIII is mapped to chromosome 1 by spot-blot analysis of sorted human chromosomes. Hybridization of Fc gamma RII and Fc gamma RIII probes to restriction digests of human genomic DNA separated by pulsed-field gel electrophoresis demonstrates physical linkage of the two genes within a maximum distance of 200 kilobases. The results identify a locus for at least two Fc gamma R genes on human chromosome 1.


Assuntos
Antígenos de Diferenciação/genética , Cromossomos Humanos Par 1 , Clonagem Molecular , Ligação Genética , Receptores Fc/genética , Sequência de Aminoácidos , Sequência de Bases , Linhagem Celular , Mapeamento Cromossômico , DNA Recombinante/isolamento & purificação , Humanos , Imunoglobulina G/metabolismo , Dados de Sequência Molecular , Receptores de IgG
4.
Immunogenetics ; 29(5): 331-9, 1989.
Artigo em Inglês | MEDLINE | ID: mdl-2565886

RESUMO

Human receptors for IgG (Fc gamma R) play important roles in the immune response. Expression of the human Fc gamma RII gene may be relevant in immune complex related disorders such as systemic lupus erythematosus and Sjogren's syndrome. We have used spot blot analysis of dual laser-sorted human chromosomes to localize the Fc gamma RII gene to human chromosome 1. Spot blot analysis of sorted derivative chromosomes sublocalized the gene to the chromosome 1 long arm (1q12----q25.1). This subchromosomal localization involved reassigning a reciprocal chromosome translocation breakpoint. We also identified Xmn I and Taq I Fc gamma RII polymorphic restriction sites that arose before the races diverged. These common Xmn I and Taq I polymorphisms are predicted to be informative for segregation analysis with human diseases in 85% of all matings.


Assuntos
Antígenos de Diferenciação/genética , Mapeamento Cromossômico , Cromossomos Humanos Par 1/ultraestrutura , Receptores Fc/genética , Evolução Biológica , Southern Blotting , Humanos , Ativação Linfocitária , Mutação , Hibridização de Ácido Nucleico , Polimorfismo de Fragmento de Restrição , Receptores de IgG
5.
Obstet Gynecol ; 72(3 Pt 2): 456-9, 1988 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-3043293

RESUMO

Chronic renal failure is strongly associated with poor pregnancy outcome. Women dependent upon hemodialysis before conception rarely achieve a successful live birth. Pregnancies in three women requiring chronic hemodialysis before conception and throughout gestation resulted in three live births, of whom one survived the neonatal period. The risks of dialysis in pregnancy (hemodialysis and peritoneal dialysis) are significant to both the mother and fetus. Polyhydramnios appears to be a major complication in women dependent upon chronic hemodialysis.


Assuntos
Falência Renal Crônica/terapia , Complicações na Gravidez/terapia , Resultado da Gravidez , Diálise Renal , Adulto , Feminino , Humanos , Gravidez , Fatores de Risco
6.
Am J Perinatol ; 5(2): 98-100, 1988 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-3348869

RESUMO

A fetal heart rate tracing that is notable for decreased short- and long-term variability is seen in association with normal umbilical cord blood gas values. A great vein of Galen aneurysm is diagnosed in the neonatal period. This case exemplifies a central nervous system disorder that is present before labor and is associated with normal oxygenation of the fetus and an abnormal fetal heart rate tracing. The causes of diminished fetal heart rate variability are discussed.


Assuntos
Veias Cerebrais , Frequência Cardíaca Fetal , Aneurisma Intracraniano/congênito , Adulto , Embolização Terapêutica , Feminino , Insuficiência Cardíaca/etiologia , Humanos , Recém-Nascido , Aneurisma Intracraniano/complicações , Aneurisma Intracraniano/fisiopatologia , Aneurisma Intracraniano/terapia , Masculino , Gravidez
9.
J Perinat Med ; 16(1): 71-5, 1988.
Artigo em Inglês | MEDLINE | ID: mdl-3042945

RESUMO

There is obvious confusion and overlap involving these various syndromes, i.e., Roberts syndrome, SC phocomelia, and TAR syndrome. However, the patient reported here seemed to exhibit the features of shortened upper extremities, clefting, and microbrachycephaly characteristic of Roberts syndrome. Antenatal detection of Roberts syndrome may be important in that early neonatal death can be expected. Other similar syndromes may have much longer survival. Cytogenetic abnormalities may be detected as well. It appears that routine ultrasonographic assessment of humerus length in addition to femur length may yield certain diagnoses that otherwise would be missed. The parents can be counselled concerning antenatal management including the possibility of not performing a cesarean section for some abnormal presentations.


Assuntos
Anormalidades Múltiplas/diagnóstico , Diagnóstico Pré-Natal , Ultrassonografia , Adulto , Fissura Palatina/diagnóstico , Orelha Externa/anormalidades , Feminino , Humanos , Úmero/anormalidades , Hidrocefalia/diagnóstico , Microcefalia/diagnóstico , Gravidez , Síndrome
10.
J Reprod Med ; 31(6): 520-2, 1986 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-3525835

RESUMO

Chorioangiomas are usually small and found by careful sectioning of the placenta. In recent years ultrasonography has been used in antenatal diagnosis. Multiple and large tumors (greater than 5 cm) are associated with increases in fetal morbidity and mortality. We treated a woman who had severe polyhydramnios and a large chorioangioma with vascular channels in the tumor confirmed by Doppler studies. Daily fetal breathing was used to monitor fetal well-being.


Assuntos
Hemangioma/diagnóstico , Doenças Placentárias/diagnóstico , Complicações Neoplásicas na Gravidez/diagnóstico , Ultrassonografia , Adulto , Feminino , Humanos , Recém-Nascido , Gravidez
11.
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...