RESUMO
We report on 2 fetuses with prenatally diagnosed mosaic isochromosome 20q in amniotic fluid. Neither had an identifiable cytogenetic abnormality after birth. One infant developed a benign intracranial dermoid cyst at age 8 months. The other was completely normal in all respects. We are aware of 13 fetuses with this prenatally diagnosed chromosome finding; all fetuses tested have had normal chromosomes on subsequent cytogenetic studies and all, except one, have been morphologically normal. Fetuses with mosaic isochromosome 20q identified on amniocentesis are most likely to be phenotypically and cytogenetically normal after birth.
Assuntos
Amniocentese , Aberrações Cromossômicas , Cromossomos Humanos Par 20 , Mosaicismo/genética , Adulto , Feminino , Humanos , LactenteRESUMO
The Meckel syndrome (MS) is an autosomal recessive disorder classically defined by the triad of occipital encephalocele, multicystic kidneys, and polydactyly. Here we describe 3 sibs with varying manifestations of MS. The propositus had isolated cystic renal disease. The other sibs were both prenatally diagnosed with renal disease, polydactyly, and the Dandy-Walker malformation, an unusual central nervous system defect in MS. These findings are discussed in the context of the phenotypic expression of MS and the nosology of this disorder and the cerebro-reno-digital (Meckel-like) syndromes.
Assuntos
Anormalidades Múltiplas/genética , Síndrome de Dandy-Walker/genética , Encefalocele/genética , Doenças Renais Policísticas/genética , Polidactilia/genética , Adulto , Feminino , Genes Recessivos , Humanos , Masculino , Osso Occipital/anormalidades , Gravidez , Síndrome , Ultrassonografia Pré-NatalRESUMO
Multiple congenital anomalies were identified at 16 weeks gestation in one fetus of an unsuspected twin pregnancy while ultrasound examination was performed before routine genetic amniocentesis. Further sonographic studies documented the amniotic band sequence (ABS) and transient oligohydramnios in the affected fetus. The latter finding supports the theory of amnion rupture followed by amniotic fluid leakage through an ineffective chorion barrier as the pathogenesis of compression related anomalies in this syndrome. Extensive craniofacial involvement including hydrocephalus, encephalocele, and multiple facial clefts in the affected fetus, combined with an erroneous ultrasound diagnosis of ABS in the unaffected twin, created an extremely difficult management and counseling situation. A review of ABS, the embryology of placental membrane development, and a discussion of selective termination procedures are presented.
Assuntos
Síndrome de Bandas Amnióticas/genética , Doenças em Gêmeos , Adulto , Síndrome de Bandas Amnióticas/etiologia , Líquido Amniótico , Cesárea , Feminino , Aconselhamento Genético , Humanos , Recém-Nascido , Idade Materna , Gravidez , Gravidez de Alto Risco , Diagnóstico Pré-Natal , Risco , Gêmeos Monozigóticos , UltrassonografiaRESUMO
We report on a newborn boy with a de novo inverted interstitial duplication of chromosome 8(q13----q24.1). This form of cytogenetic abnormality, in which a mirror image interstitial duplication has occurred, is exceedingly rare. Review of the literature and mechanisms to explain the origin of this type of chromosome aberration are presented. A review of the findings from individuals with partial dup(8q) demonstrate remarkable similarity to the infant we describe.
Assuntos
Aberrações Cromossômicas/genética , Inversão Cromossômica , Cromossomos Humanos Par 8/ultraestrutura , Ossos Faciais/anormalidades , Genitália Masculina/anormalidades , Humanos , Hipertelorismo , Recém-Nascido , Masculino , Crânio/anormalidades , Tetralogia de FallotRESUMO
Prenatal diagnosis of a posterior nuchal cystic hygroma was made at 13 weeks of gestation in a fetus diagnosed at birth with Noonan syndrome. Through serial sonographic evaluation during pregnancy, the embryologic evolution of cystic hygroma into nuchal skin thickening was appreciated and later correlated with postnatal findings of nuchal skin fold redundancy and pterygium colli in a patient with Noonan syndrome. These observations support the concept of the jugular lymphatic disruption sequence as pathogenesis of the nuchal findings in severely affected Noonan syndrome patients.
Assuntos
Linfangioma/diagnóstico por imagem , Síndrome de Noonan/diagnóstico por imagem , Ultrassonografia Pré-Natal , Adulto , Feminino , Humanos , Regressão Neoplásica Espontânea , GravidezRESUMO
We describe a fourth generation of involvement with hand-foot-genital syndrome. The first 3 generations of this family, which included 5 affected females and no affected males, were reported previously by Verp et al. [1983]. In the fourth generation, 2 affected males are identified. To our knowledge, the findings of bilateral vesicoureteral reflux in one boy and bilateral ureteropelvic junction obstruction in his cousin represent the first reports of urinary tract abnormalities in males with this syndrome.
Assuntos
Deformidades Congênitas do Pé/genética , Deformidades Congênitas da Mão/genética , Hipospadia/genética , Sistema Urinário/anormalidades , Adulto , Pré-Escolar , Feminino , Humanos , Recém-Nascido , Masculino , Linhagem , Gravidez , Complicações na Gravidez , SíndromeRESUMO
A male fetus with decreased calvarial mineralization and suspected omphalocele was identified prenatally in a woman with oligohydramnios and Melnick-Needles syndrome (MNS). At autopsy, exophthalmos, prune belly sequence with urethal atresia and megacystis, tetralogy of Fallot, atrioventricular canal defect, and complete malrotation of the gut were identified. Mandibular hypoplasia and delicate, bowed, irregular, long bones and ribs with widening and deep cupping of the metaphyses were found radiographically. In addition, we review 3 previously reported cases of males with similar, lethal malformations, all born to mothers with MNS. It is our conclusion that these anomalies characterize the male MNS phenotype. A review of all reported viable individuals with MNS identified 2 distinct entities: a mild form found only in females, compatible with normal life expectancy in most cases and inherited in an X-linked dominant male lethal or sex limited autosomal dominant pattern, and a different, more severe disorder, termed precocious osteodysplasty, found in both males and females and inherited as an autosomal recessive trait.
Assuntos
Osteocondrodisplasias/genética , Adulto , Feminino , Genes Dominantes , Genes Letais , Ligação Genética , Cardiopatias Congênitas/genética , Humanos , Masculino , Osteocondrodisplasias/classificação , Osteocondrodisplasias/diagnóstico , Linhagem , Gravidez , Diagnóstico Pré-Natal , Síndrome do Abdome em Ameixa Seca/genética , Cromossomo XRESUMO
In our consecutive series of 2,574 chorionic villus sampling (CVS) patients, 146 women (5.7%) underwent a subsequent amniocentesis in the same pregnancy for the indications of absent or insufficient villi (3.3%), elevated maternal serum alpha-fetoprotein (0.93%), CVS mosaicism (0.89%), culture failure (0.23%), specimen contamination (0.15%), and CVS aneuploidy (0.12%). Patients presenting for a CVS should be informed of the possible need for a subsequent amniocentesis in the same pregnancy. There is a need for individual prenatal diagnosis programs to analyze their own data and provide genetic counseling information which pertains specifically to their institution.
Assuntos
Amniocentese , Amostra da Vilosidade Coriônica , Amniocentese/efeitos adversos , Amniocentese/estatística & dados numéricos , Amostra da Vilosidade Coriônica/efeitos adversos , Feminino , Morte Fetal/etiologia , Doenças Fetais/diagnóstico , Doenças Fetais/genética , Aconselhamento Genético , Doenças Genéticas Inatas/diagnóstico , Humanos , Mosaicismo , Gravidez , Complicações na Gravidez/sangue , alfa-Fetoproteínas/análiseRESUMO
Eighteen girls with Aicardi syndrome were identified through a survey of neurologists, geneticists, and ophthalmologists. All had infantile seizures, developmental delay, agenesis of the corpus callosum (complete: 72%, partial: 28%), and characteristic chorioretinal lacunar lesions. Costovertebral defects including hemivertebrae, scoliosis, and absent or malformed ribs were present in 39%, cortical heterotopias were present in 50%, and microphthalmia was identified in a third. Cytogenetic investigation was carried out in all families. An unbalanced X;3 translocation, 46,X,der(X)t(X;3)(p22.3;p23)mat, was discovered in a girl with chorioretinal lacunar lesions characteristic of Aicardi syndrome, developmental delay, and infantile seizures. However, this child had a normal appearing corpus callosum on CT and magnetic resonance imaging scans and therefore did not meet the criteria for inclusion in the study. Chromosomes of all other patients and parents were normal. Findings at birth, age of seizure onset, treatment, and prognosis are discussed. The pedigree data from these 18 families demonstrated an unaffected male:female sib ratio of 1:1.7 and a 14% spontaneous abortion rate. The findings of this study support the contention that Aicardi syndrome is an X-linked dominant disorder with early embryonic lethality in hemizygous males and that all cases represent new mutations.
Assuntos
Anormalidades Múltiplas/patologia , Agenesia do Corpo Caloso , Cromossomos Humanos Par 3 , Oftalmopatias/congênito , Linhagem , Convulsões/congênito , Translocação Genética , Cromossomo X , Anormalidades Múltiplas/genética , Criança , Pré-Escolar , Bandeamento Cromossômico , Oftalmopatias/diagnóstico , Feminino , Genes Dominantes , Humanos , Cariotipagem , Imageamento por Ressonância Magnética , Gravidez , Prognóstico , Convulsões/diagnóstico , Convulsões/tratamento farmacológico , Síndrome , Tomografia Computadorizada por Raios XRESUMO
We present a 4-year-old girl with a maternally derived, unbalanced X;3 translocation resulting in partial Xp monosomy and partial 3p trisomy. She had chorioretinal defects, developmental delay, infantile seizures, and microphthalmia. These findings initially suggested a diagnosis of Aicardi syndrome. However, she had a normal-appearing corpus callosum on CT and magnetic resonance imaging scans of the brain and her retinal findings were not typical for Aicardi syndrome. This represents the 6th reported example of microphthalmia associated with an Xp22 chromosome abnormality. Four of these individuals also had features suggestive of focal dermal hypoplasia (FDH), which was not evident in our patient. The available evidence supports the hypothesis that gene disruption at Xp22 may lead to findings similar to those seen in Aicardi syndrome and FDH, both of which are believed to be X-linked dominant male lethal conditions.
Assuntos
Corioide/anormalidades , Microftalmia/genética , Retina/anormalidades , Translocação Genética , Cromossomo X , Pré-Escolar , Deleção Cromossômica , Cromossomos Humanos Par 3 , Feminino , Humanos , Cariotipagem , Síndrome , TrissomiaRESUMO
BACKGROUND: Therapeutic amniocentesis has been performed traditionally by gravitational drainage or syringe aspiration. We describe a technique for relatively rapid, large-volume therapeutic amniocentesis using a negative-pressure vacuum bottle aspiration system. TECHNIQUE: The procedure involves insertion of a 20-gauge spinal needle into the amniotic cavity followed by connection to a 1-L vacuum bottle via noncollapsible tubing. EXPERIENCE: During a 5-year period, 86 therapeutic amniocenteses were performed on 26 women. The amniotic fluid removal rate was 89 mL/minute. There were three instances of transient preterm labor, three cases of ruptured membranes within a week of the procedure, and no cases of abruption, chorioamnionitis, or fetal distress. CONCLUSION: The vacuum bottle aspiration technique for therapeutic amniocentesis permits expeditious removal of large volumes of amniotic fluid safely and effectively.
Assuntos
Amniocentese/métodos , Complicações na Gravidez/terapia , Sucção/métodos , Amniocentese/efeitos adversos , Feminino , Humanos , Gravidez , VácuoRESUMO
BACKGROUND: Suicide attempts during pregnancy are rare. Over-the-counter and psychotropic medications are most commonly used. Although intentional overdose of haloperidol has been reported in nonpregnant adults, it has not, to our knowledge, been reported previously during pregnancy. In this case of suicide attempt by haloperidol overdose, maternal and fetal responses were studied extensively. CASE: Intentional ingestion of 300 mg haloperidol by a pregnant woman at 34 weeks' gestation caused maternal unresponsiveness, an extrapyramidal reaction, temporary fetal akinesia, and a nonreactive nonstress test. The mother recovered in 48 hours. The fetus did not reach a biophysical profile score of ten until 5 days after presentation. CONCLUSION: Haloperidol overdose during pregnancy causes a maternal extrapyramidal reaction, temporary fetal akinesia, and prolonged fetal neuromuscular depression.
Assuntos
Antipsicóticos/intoxicação , Haloperidol/intoxicação , Complicações na Gravidez/psicologia , Tentativa de Suicídio , Adulto , Antipsicóticos/administração & dosagem , Overdose de Drogas , Feminino , Doenças Fetais/induzido quimicamente , Haloperidol/administração & dosagem , Humanos , GravidezRESUMO
OBJECTIVE: To determine the incidence of chromosomal abnormality in sonographically normal fetuses after amniocentesis for elevated maternal serum alpha-fetoprotein (MSAFP), and to compare the spectrum of abnormality with that seen in women undergoing amniocentesis for advanced maternal age. METHODS: Cytogenetic and sonographic findings from women undergoing amniocentesis for elevated MSAFP (at least 2.0 multiples of median) between 1988-1992 were reviewed retrospectively. The literature was reviewed and data compiled regarding the risk of chromosomal abnormality for women with elevated MSAFP levels. RESULTS: The incidence of abnormal karyotype among all women with elevated MSAFP was 1.23% (nine of 733). The risk of an abnormal karyotype with a normal ultrasound examination was 1.01% (seven of 696). This included three fetuses with sex chromosome abnormalities, three with de novo, apparently balanced rearrangements, and one with an unbalanced structural rearrangement. CONCLUSIONS: The risk of chromosomal abnormality in nonselected patients, predominantly younger than 35 years of age, with elevated MSAFP and a sonographically normal fetus is 0.6%, based on a compilation of our data and reports published previously. The spectrum of abnormality in women with elevated MSAFP differs from that in women of advanced maternal age. Patients should be specifically counseled regarding this difference.
Assuntos
Aberrações Cromossômicas/epidemiologia , Doenças Fetais/epidemiologia , Ultrassonografia Pré-Natal , alfa-Fetoproteínas/análise , Adulto , Amniocentese , Aberrações Cromossômicas/genética , Transtornos Cromossômicos , Feminino , Doenças Fetais/genética , Humanos , Incidência , Cariotipagem , Idade Materna , Gravidez , Estudos Retrospectivos , Fatores de RiscoRESUMO
Elective induction of labor, followed by vaginal delivery, was carried out at 25 to 39 weeks' gestation in 14 consecutive patients (15 pregnancies) with an anencephalic fetus. Laminaria tents and prostaglandin drugs were used. The procedures produced no serious untoward effects and required only 3 hospital days.
Assuntos
Aborto Induzido , Anencefalia , Parto Obstétrico , Feminino , Humanos , Laminaria , Gravidez , Prostaglandinas E/uso terapêutico , Prostaglandinas F/uso terapêuticoRESUMO
OBJECTIVE: To determine the distribution of nuchal skinfold thickness in normal and Down syndrome pregnancies and to evaluate the use of this sonographic measurement as a screening test for fetal Down syndrome. METHODS: A prospective, multicenter, population-based study was performed by experienced obstetric sonographers on 1382 women with sonographically normal fetuses undergoing second-trimester amniocentesis for the indication of advanced maternal age. A standard, well-defined sonographic image was obtained at all collaborating centers. The distributions of nuchal skinfold thickness were compared between euploid and Down syndrome fetuses. RESULTS: There were 1346 chromosomally normal pregnancies, 13 fetuses with Down syndrome (1:106), and 23 other chromosome abnormalities. Seventeen fetuses had measurements of 6 mm or greater, and one of these had Down syndrome. The median nuchal skinfold thickness in Down syndrome was 3.2 mm and in euploid fetuses was 3.1 mm. By the Mann-Whitney rank-sum test, there was no statistically significant difference in nuchal skinfold between the euploid and Down syndrome fetuses (P = .5). Overall, using a nuchal skinfold thickness of 6 mm or greater as a screening test, the detection rate for Down syndrome was one of 13 (8%), the false-positive rate was 16 of 1382 (1.2%), the positive predictive value was one of 17 (6%), and the probability of detecting Down syndrome was 6.5%. CONCLUSION: In this investigation, excess nuchal skinfold thickness was a poor and unreliable screening test for Down syndrome.
Assuntos
Síndrome de Down/diagnóstico por imagem , Dobras Cutâneas , Ultrassonografia Pré-Natal , Adulto , Amniocentese , Feminino , Humanos , Idade Materna , Pessoa de Meia-Idade , Pescoço/diagnóstico por imagem , Valor Preditivo dos Testes , Gravidez , Gravidez de Alto Risco , Estudos ProspectivosRESUMO
It has been established that the finding of a fetal choroid plexus cyst confers an increased risk of aneuploidy, predominantly trisomy 18. In view of this association many investigators have advocated amniocentesis when a choroid plexus cyst is identified by prenatal ultrasonography. A risk/benefit and economic analysis of such a policy is presented. When the following factors are taken into account-published data on the frequency of isolated choroid plexus cysts in second trimester fetuses, the risk of trisomy 18 in these fetuses, the population frequency of trisomy 18, the natural history and prognosis for these infants, and the risks and cost of amniocentesis--it is concluded that performing amniocentesis on second trimester fetuses with choroid plexus cysts is neither cost effective nor beneficial. For the detection of one infant with trisomy 18 that will survive past five months, 25 normal fetuses would be lost owing to amniocentesis. Identification of trisomy 18 by determining the presence of choroid plexus cysts in fetuses is not a worthwhile screening policy.
Assuntos
Encefalopatias/diagnóstico por imagem , Plexo Corióideo , Cromossomos Humanos Par 18 , Cistos/diagnóstico por imagem , Trissomia , Ultrassonografia Pré-Natal , Aneuploidia , Biomarcadores/sangue , Encefalopatias/embriologia , Encefalopatias/prevenção & controle , Gonadotropina Coriônica/sangue , Cistos/embriologia , Cistos/prevenção & controle , Estriol/sangue , Feminino , Humanos , Programas de Rastreamento , Gravidez , alfa-Fetoproteínas/análiseRESUMO
Oligohydramnios is a relatively common complication of pregnancy. Etiologies include congenital anomalies, intrauterine growth retardation, premature rupture of the membranes, drugs, postterm gestation and postmaturity. Sequelae from prolonged oligohydramnios including pulmonary hypoplasia and fetal compression syndrome can be devastating. Perinatal morbidity and mortality are both significantly increased in pregnancies complicated by oligohydramnios. Successful management requires a thorough search for the cause of the decreased amniotic fluid volume, and close antenatal surveillance.
Assuntos
Oligo-Hidrâmnio/etiologia , Feminino , Humanos , Mortalidade Infantil , Recém-Nascido , Oligo-Hidrâmnio/diagnóstico , Oligo-Hidrâmnio/terapia , Gravidez , Resultado da Gravidez , Ultrassonografia Pré-NatalRESUMO
Normal fetal growth and development during pregnancy is highly dependent upon adequate fetal movement. Limitation of movement, regardless of the underlying cause, can result in a particular pattern of abnormal fetal morphogenesis. This phenotype is termed the fetal akinesia deformation sequence (FADS). The etiology of fetal akinesia may be generally classified into one of five categories: neuropathy, myopathy, restrictive dermopathy, teratogen exposure, or restricted movement due to intrauterine constraint. In this article, the differential diagnosis of fetal akinesia is systematically reviewed and information regarding prenatal diagnosis, prognosis, perinatal management, and recurrence risks are discussed.
Assuntos
Movimento Fetal , Anormalidades Congênitas/classificação , Anormalidades Congênitas/diagnóstico , Anormalidades Congênitas/etiologia , Diagnóstico Diferencial , Humanos , PrognósticoRESUMO
Ovarian cancer is the fifth most common malignancy among American women and the fourth leading cause of cancer death. The rapid advances in molecular genetic analysis, presymptomatic detection, and treatment of ovarian cancer are staggering. In this review, both the genetic component and the molecular biology of ovarian cancer are discussed, as well as current recommendations for genetic counseling. It is important for the practicing obstetrician and gynecologist to become familiar with these concepts, for it is he or she who will likely serve as a primary resource of information for these patients.
Assuntos
Neoplasias Ovarianas/genética , Neoplasias da Mama/genética , Neoplasias Colorretais Hereditárias sem Polipose/complicações , Feminino , Genes BRCA1 , Genes Supressores de Tumor , Aconselhamento Genético , Humanos , Mutação , Proto-OncogenesRESUMO
Intrauterine irrigation with a cefazolin solution at cesarean section was compared with intravenous cefazolin administration for prophylaxis against post-cesarean-section endomyometritis in a randomized, controlled, prospective fashion. There were no statistically significant differences in the incidence of infection between the lavage and intravenous groups. The incidence of endomyometritis was 37% in the lavage group and 29% in the intravenous (P = NS). Intrauterine cefazolin lavage is safe, effective, time saving and more cost effective than intravenous cefazolin in preventing post-cesarean-section endomyometritis.