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1.
Ultrasound Obstet Gynecol ; 30(2): 221-6, 2007 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-17582228

RESUMO

A series of five cases of skeletal dysplasia is reported in which the diagnosis was reached at the 11-14-week routine ultrasound examination in our referral center. All five cases had increased nuchal translucency thickness (NT) associated with bone abnormalities. We review the current literature on skeletal dysplasia in the first trimester of pregnancy associated with increased NT.


Assuntos
Anormalidades Musculoesqueléticas/diagnóstico por imagem , Medição da Translucência Nucal , Aborto Eugênico , Adulto , Feminino , Humanos , Gravidez , Primeiro Trimestre da Gravidez
2.
J Gynecol Obstet Biol Reprod (Paris) ; 34 Spec No 1: 3S146-51, 2005 Apr.
Artigo em Francês | MEDLINE | ID: mdl-15980784

RESUMO

METHODS: We conducted a PubMed research using the following key words: fetal, smoking, distress, hypoxia, acidosis, heart rate, cesarean. RESULTS: The different combinations of key works allowed selection of 251 since 1967. Several article were addressed directly to the question raised; two for meconial fluid alone. One article detailed possible method biases. Several articles detailed the Apgar score in newborns of smoking mothers. Three calculated the risk of cesarean section in smokers. CONCLUSION: Data in the literature is not sufficient to argue in favor of an association between fetal asphyxia during labor and smoking. Only one study showed a higher rate of cesarean section in mothers smoking more than 10 cigarettes per day. Nevertheless, the Apgar score does not appear to be modified by moderate maternal smoking. Paradoxically, maternal smoking could have a protective effect on meconial aspiration and could have a moderately reducing effect on the rate of cesarean section during labor in patients smoking less than 10 cigarettes per day via lower fetal weight. These findings should be examined with caution because they still need to be confirmed and do not take into consideration other adverse effects of smoking on the fetus.


Assuntos
Acidose/etiologia , Parto Obstétrico , Doenças Fetais/etiologia , Hipóxia/etiologia , Fumar/efeitos adversos , Índice de Apgar , Cesárea/estatística & dados numéricos , Feminino , Frequência Cardíaca Fetal/efeitos dos fármacos , Humanos , Recém-Nascido , Síndrome de Aspiração de Mecônio/epidemiologia , Gravidez
3.
Prenat Diagn ; 23(1): 25-30, 2003 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-12533808

RESUMO

Congenital erythropoietic porphyria (CEP) or Günther's disease is the rarest form of the porphyrias. The disease is usually diagnosed at birth or during early infancy, but rarely in utero. We describe here the first two cases of very early prenatal expression of CEP with cystic hygroma diagnosed at 14 weeks in the first fetus and at 19 weeks in the second. Both fetuses presented with severe nonimmune hydrops fetalis as early as 19 and 22 weeks, associated with intrauterine growth retardation, hyperechogenic kidneys and bones. Amniotic fluid was dark brown and uro- and coproporphyrin I was dramatically increased. Molecular screening of the CEP gene detected heterozygous C73R mutation in both fetuses, the other parental mutation being as yet unknown.


Assuntos
Neoplasias de Cabeça e Pescoço/diagnóstico , Linfangioma Cístico/diagnóstico , Porfiria Eritropoética/diagnóstico , Aborto Eugênico , Adulto , Amniocentese , Líquido Amniótico/química , Coproporfirinas/análise , Feminino , Doenças Fetais/diagnóstico por imagem , Retardo do Crescimento Fetal/diagnóstico por imagem , Retardo do Crescimento Fetal/etiologia , Idade Gestacional , Neoplasias de Cabeça e Pescoço/complicações , Heterozigoto , Humanos , Hidropisia Fetal/diagnóstico por imagem , Hidropisia Fetal/etiologia , Nefropatias/diagnóstico por imagem , Nefropatias/etiologia , Linfangioma Cístico/complicações , Mutação , Porfiria Eritropoética/complicações , Porfiria Eritropoética/genética , Gravidez , Ultrassonografia Pré-Natal , Uroporfirinas/análise
4.
Eur J Obstet Gynecol Reprod Biol ; 70(1): 101-5, 1996 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-9031929

RESUMO

OBJECTIVE: To study the mechanism of action of prostaglandin E2 (PGE2) and its analogue sulprostone leading to production of glycosaminoglycans (GAGs) in the human uterine cervix. STUDY DESIGN: We analysed the effects of PGE2 and its analogue sulprostone upon production of adenosine 3',5'-monophosphate (cAMP), in human cultured fibroblasts. We also studied the effects of PGE2, sulprostone and a cAMP analogue (8-Bromo-cAMP), on the incorporation of [3H]glucosamine into GAGs in human cervical fibroblasts in culture. RESULTS: Following treatment with PGE2 (10(-4)-10(-6) M), we observed a significant increase in the production of cAMP from 96.3 +/- 8.4 pmol/10(6) cells without phosphodiesterase inhibitor 3-isobutyl-methylxanthine (IBMX) to 325 +/- 63 pmol/10(6) cells with 10(-4) M IBMX (Spearman correlation test; P < 0.05). Under the same conditions, the effects of sulprostone (10(-6) M) were limited (from 8.1 +/- 1.5 to 51.3 +/- 14.1 pmol/10(6) cells without and with IBMX, respectively; not significant). Both PGE2 and 8-bromo-cAMP (from 10(-12) to 10(-4) M) increased [3H]glucosamine uptake into GAGs (Spearman correlation test; P < 0.05). Sulprostone (10(-12)-10(-4) M) was unable to reproduce such an effect even after a 24 or 48 h treatment. CONCLUSION: Since firstly, PGE2 acts through EP1, EP2 and EP3 specific receptors, whereas the action of sulprostone is only mediated by EP1 and EP3, and secondly EP2 receptor is coupled with cAMP production, we conclude that cAMP is involved in mediating the action of PGE2 upon GAG synthesis by human cultured cervical fibroblasts.


Assuntos
Colo do Útero/metabolismo , AMP Cíclico/farmacologia , Dinoprostona/farmacologia , Glicosaminoglicanos/biossíntese , 1-Metil-3-Isobutilxantina/farmacologia , 8-Bromo Monofosfato de Adenosina Cíclica/farmacologia , Células Cultivadas , Colo do Útero/citologia , Colo do Útero/efeitos dos fármacos , AMP Cíclico/biossíntese , Dinoprostona/análogos & derivados , Feminino , Fibroblastos/metabolismo , Glucosamina/metabolismo , Humanos , Trítio
5.
Hum Reprod ; 8(11): 1796-806, 1993 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-7507128

RESUMO

Oestradiol is important in the growth of uterine leiomyomata and may act primarily or secondarily through mediators such as growth factors, including the insulin-like growth factors (IGF-I and IGF-II), mitogenic peptides. IGF binding proteins (IGFBPs) modulate IGF actions at their target cells. The objective of this study was to examine the possible steroid dependence of IGF, IGFBP and IGF receptor gene expression and IGFBP synthesis in uterine leiomyomata, using tissues from women cycling normally and made hypo-oestrogenic by a gonadtrophin-releasing hormone agonist (GnRHa). Using a solution hybridization ribonuclease protection assay, anti-sense RNA probes for IGF-I, IGF-II and beta-actin (control) were hybridized with total RNA isolated from leiomyomata exposed in vivo to a range of serum oestradiol (< 40-240 pg/ml) and progesterone (0-10 ng/ml) concentrations. IGF-I gene expression was most abundant in leiomyomata obtained during the late proliferative phase of the cycle and was undetectable in leiomyomata from hypo-oestrogenic patients. IGF-II gene expression was not dependent on endogenous steroid concentrations or cycle stage. IGFBP gene expression was investigated by Northern blotting. The order of relative abundance of IGFBP mRNAs was IGFBP-4 >>> IGFBP-3 >> IGFBP-5 > IGFBP-2 and was not dependent on the in-vivo oestrogen status. Type I and type II IGF receptor gene expression was investigated by polymerase chain reaction using gene-specific primers. Type I and type II IGF receptor mRNAs were detected in leiomyomata and were not dependent on cycle stage or in-vivo oestrogen status. Explant cultures of leiomyomata and myometrium synthesized IGFBP-3 (mol. wt = 38-43 kDa), IGFBP-4, and binding proteins of mol. wt = 34 and 31 kDa. Identification of IGFBP-2 was inconclusive, and IGFBP-1 was not detected. These data support the hypothesis that IGF-I, but not IGF-II, may be a mediator of oestradiol action in the growth of uterine leiomyomata, and that IGFBPs may further modulate, by an autocrine or paracrine mechanism, IGF-I action in this tissue.


Assuntos
Proteínas de Transporte/genética , Expressão Gênica , Leiomioma/metabolismo , Receptor IGF Tipo 1/genética , Receptor IGF Tipo 2/genética , Somatomedinas/genética , Neoplasias Uterinas/metabolismo , Sequência de Bases , Northern Blotting , Proteínas de Transporte/biossíntese , Estradiol/sangue , Feminino , Humanos , Proteínas de Ligação a Fator de Crescimento Semelhante a Insulina , Fator de Crescimento Insulin-Like I/genética , Fator de Crescimento Insulin-Like II/genética , Dados de Sequência Molecular , Reação em Cadeia da Polimerase , Progesterona/sangue , Sondas RNA
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