RESUMO
OBJECTIVE: Lifestyle intervention could help obese pregnant women to limit their weight gain during pregnancy and improve their psychological comfort, but has not yet been evaluated in randomized controlled trials. We evaluated whether a targeted antenatal lifestyle intervention programme for obese pregnant women influences gestational weight gain (GWG) and levels of anxiety or depressed mood. DESIGN AND SUBJECTS: This study used a longitudinal interventional design. Of the 235 eligible obese pregnant women, 205 (mean age (years): 29±4.5; body mass index (BMI, kg m(-)(2)): 34.7±4.6) were randomized to a control group, a brochure group receiving written information on healthy lifestyle and an experimental group receiving an additional four antenatal lifestyle intervention sessions by a midwife trained in motivational lifestyle intervention. Anxiety (State and Trait Anxiety Inventory) and feelings of depression (Edinburgh Depression Scale) were measured during the first, second and third trimesters of pregnancy. Socio-demographical, behavioural, psychological and medical variables were used for controlling and correcting outcome variables. RESULTS: We found a significant reduction of GWG in the brochure (9.5 kg) and lifestyle intervention (10.6 kg) group compared with normal care group (13.5 kg) (P=0.007). Furthermore, levels of anxiety significantly decreased in the lifestyle intervention group and increased in the normal care group during pregnancy (P=0.02); no differences were demonstrated in the brochure group. Pre-pregnancy BMI was positively related to levels of anxiety. Obese pregnant women who stopped smoking recently showed a significant higher GWG (ß=3.04; P=0.01); those with concurrent gestational diabetes mellitus (GDM) (ß=3.54; P=0.03) and those who consumed alcohol on a regular base (ß=3.69; P=0.04) showed significant higher levels of state anxiety. No differences in depressed mood or obstetrical/neonatal outcomes were observed between the three groups. CONCLUSIONS: A targeted lifestyle intervention programme based on the principles of motivational interviewing reduces GWG and levels of anxiety in obese pregnant women.
Assuntos
Ansiedade/prevenção & controle , Depressão/prevenção & controle , Estilo de Vida , Obesidade/terapia , Complicações na Gravidez/terapia , Cuidado Pré-Natal/métodos , Aumento de Peso , Adulto , Ansiedade/epidemiologia , Bélgica/epidemiologia , Índice de Massa Corporal , Depressão/epidemiologia , Feminino , Conhecimentos, Atitudes e Prática em Saúde , Humanos , Estudos Longitudinais , Motivação , Obesidade/epidemiologia , Obesidade/prevenção & controle , Obesidade/psicologia , Educação de Pacientes como Assunto , Gravidez , Complicações na Gravidez/epidemiologia , Complicações na Gravidez/prevenção & controle , Complicações na Gravidez/psicologia , Prevalência , Fatores de Risco , Comportamento de Redução do Risco , Inquéritos e QuestionáriosRESUMO
Congenital High Airway Obstruction Syndrome (CHAOS) is a potential lethal condition. We describe a case report of CHAOS, with additional malformations diagnosed at 20 weeks. Autopsy findings are suggestive for Fraser syndrome (cryptophthalmos-syndactyly syndrome; OMIM 219000). The diagnosis was confirmed by mutation analysis of FRAS1.
Assuntos
Feto Abortado/patologia , Obstrução das Vias Respiratórias/patologia , Síndrome de Fraser/diagnóstico , Adulto , Obstrução das Vias Respiratórias/congênito , Obstrução das Vias Respiratórias/diagnóstico por imagem , Autopsia , Feminino , Síndrome de Fraser/complicações , Síndrome de Fraser/genética , Humanos , Gravidez , Síndrome , Ultrassonografia Pré-NatalRESUMO
Hydrometrocolpos, occurring in approximately 1/6000 newborn girls, can be caused by a stenotic urogenital sinus, a severe cloacal malformation, but also by other conditions such as an imperforate hymen, a midline vaginal septum and vaginal atresia. The prenatal differential diagnosis of this wide spectrum of conditions is not easy and requires a multidisciplinary approach with follow-up scans and MRI to access the severity of the condition. A non-consanguineous couple was referred in the first pregnancy at 30 weeks. The father, 30 years of age, of Kaukasian origin, and the mother of Asian origin, 26 years of age. Ultrasound at 30 weeks revealed ambiguous genitalia (with suspicion of clitoral hypertrophy), a septated structure located behind the bladder compatible with hydrometrocolpos with a uterine malformation (uterus didelphys), a single umbilical artery, mild ascites and growth on the tenth centile. The differential diagnosis included a vaginal atresia, a urogenital sinus and a more severe cloacal malformation. After serial scans, MRI and counselling by an experienced surgeon the preferential diagnosis of a cloacal malformation was made and a late pregnancy termination was performed. Pathological examination revealed: low vaginal atresia with uterus didelphys, anal atresia with rectovaginal fistula and a normal urinary tractus. The differential diagnosis between hydrometrocolpos due to vaginal atresia or due to a more severe cloacal malformation is not straightforward. Care should be taken in decision making and counselling patients with these complex prenatal malformations.
Assuntos
Anormalidades Múltiplas/diagnóstico , Anus Imperfurado/diagnóstico , Cloaca/anormalidades , Doenças Fetais/diagnóstico , Cardiopatias Congênitas/diagnóstico , Hidrocolpos/diagnóstico , Polidactilia/diagnóstico , Doenças Uterinas/diagnóstico , Doenças Vaginais/diagnóstico , Anormalidades Múltiplas/embriologia , Aborto Eugênico/métodos , Adulto , Cloaca/diagnóstico por imagem , Diagnóstico Diferencial , Feminino , Cardiopatias Congênitas/embriologia , Humanos , Hidrocolpos/embriologia , Polidactilia/embriologia , Gravidez , Terceiro Trimestre da Gravidez , Ultrassonografia Pré-Natal/métodos , Doenças Uterinas/embriologia , Útero/anormalidades , Útero/diagnóstico por imagem , Útero/embriologia , Vagina/anormalidades , Vagina/diagnóstico por imagem , Vagina/embriologia , Doenças Vaginais/embriologiaRESUMO
A good pregnancy outcome is partly determined by a women's preconceptional health and healthy lifestyle. The access to prenatal care is good nowadays but the incidence of congenital malformations, preterm births, low birth weight and maternal mortality has not significantly declined over the years. Although most women of reproductive age have a gynecological examination every two years in Belgium, they are not often counseled before starting a pregnancy. The American College of Obstetricians and Gynecologists (ACOG) states that optimizing a woman's health before and between pregnancies must be an ongoing process. The most vulnerable period for fetal defects is between 4 and 10 weeks of gestation, the period of embryogenesis, meaning that counseling for a healthy life style and reducing high-risk conditions should start preferably before conception.
Assuntos
Aconselhamento , Cuidado Pré-Concepcional/métodos , Bélgica , Controle de Doenças Transmissíveis , Anticoncepção , Feminino , Aconselhamento Genético , Humanos , Estilo de Vida , Gravidez , Gravidez de Alto Risco , Fatores de RiscoAssuntos
Fístula Artério-Arterial/congênito , Cistos/diagnóstico por imagem , Transfusão Feto-Fetal/diagnóstico por imagem , Cardiopatias Congênitas/diagnóstico por imagem , Gravidez de Trigêmeos , Doenças Uterinas/diagnóstico por imagem , Diagnóstico Diferencial , Feminino , Humanos , Gravidez , Ultrassonografia Pré-NatalRESUMO
This is a retrospective review of all collected amniotic fluid samples, chorionic villus samples and other fluid-aspirations (hygroma colli fluid/urine from megacystis) over an 11-year period (1996-2006) in a single Genetic Center (University Hospital Gasthuisberg, Leuven), looking at the prenatal diagnosis of trisomy 21. In this study a total of 404 diagnoses of trisomy 21 were made on 29696 samples (1.4%). The prenatal diagnosis of trisomy 21 increased over the years with 0.88% (21/2363) in 1996 and 1.99% (50/2512)in 2006. Also the type of invasive testing changed over the years with an increase of the proportion of trisomy 21- diagnoses by chorionic villussampling from 2001. Looking at the registry for perinatal activities in Flanders for the year 2006 the live birth incidence for trisomy 21 was 1/1782 and this is lower than the often reported incidence oftrisomy 21 at birth of 1/800: it is likely that the use of more sensitive screening methods for the prenatal detection of trisomy 21 and the election of termination for most affected pregnancies affects the birth incidence oftrisomy 21.
Assuntos
Síndrome de Down/diagnóstico , Diagnóstico Pré-Natal , Adulto , Amniocentese/estatística & dados numéricos , Bélgica/epidemiologia , Amostra da Vilosidade Coriônica/estatística & dados numéricos , Síndrome de Down/epidemiologia , Feminino , Humanos , Incidência , Masculino , Idade Materna , Gravidez , Diagnóstico Pré-Natal/métodos , Diagnóstico Pré-Natal/estatística & dados numéricos , Estudos RetrospectivosRESUMO
OBJECTIVE: To assess the prenatal diagnosis of skeletal dysplasias in a single center over a ten-years period. METHODS: All antenatal detected skeletal dysplasias during the period January 1st 1996 until December 31 2005 (10 years) were retrieved from the genetic database. This database includes all skeletal dysplasias where invasive prenatal diagnosis (chorionic villus sampling/amniocentesis) was performed. The final diagnosis was sought on the basis of fetopathological examination, radiographic studies and if possible molecular testing. RESULTS: A total of 46 antenatal skeletal dysplasias were diagnosed during this period. Follow-up was only available in 38 cases. The other 8 cases involved prenatally presumed lethal skeletal dysplasias that were interrupted in the referral hospital with no further information sent to us. The mean gestational age at diagnosis was 23 weeks (range 12-33 weeks). A diagnosis < or = 24 weeks was made in 25 cases (65.8%). Eleven skeletal dysplasias were diagnosed > 30 weeks (29%) and these included all achondroplasias (n = 6), hypophosphatasia (n = 1), Jeune syndrome (n = 1), osteogenesis imperfecta type II (n = l), type I (n = 1) and type III (n = 1). In 27 cases a lethal skeletal dysplasia was present (71%) and these were all correctly predicted. Of the lethal skeletal dysplasias 5 cases were diagnosed only after 24 weeks of pregnancy (19%) and 3 were only referred after 30 weeks (11.5%). A final diagnosis was obtained in 36 cases by fetopathological examination and radiographic studies and molecular testing as deemed necessary. Specific diagnoses included: achondroplasia (n = 6), achondrogenesis (n = 2), osteogenesis imperfecta type II (n = 9), osteogenesis imperfecta type I (n = 1), osteogenesis imperfecta type III (n = 1), thanatophoric dysplasia (n = 7), hypophosphatasia (n = 1), Majewski syndrome (n = 11), Mohr-Majewski syndrome (n = 11), Jeune syndrome (n = 2), Ellis-van Creveld syndrome (n = 2), Roberts syndrome (n = 1), campomelic dysplasia (n = 2). In two cases postnatal investigation revealed no certain diagnosis and these included one patient with symmetrical tetraphocomelia with aspects of Roberts and Femur-fibula-Ulna syndrome and one patient at 15 weeks with a lethal skeletal dysplasia with rhizomelic limb shortening, a narrow thorax, platyspondyly, normocephaly, a normal pelvis, and a posterior cleft palate. A correct antenatal diagnosis was made in 25 cases (65.8%) including osteogenesis imperfecta type II (n = 9), thanatophoric dysplasia (n = 7), achondroplasia (n = 6), achondrogenesis (n = 2) and Roberts syndrome (n = 1). CONCLUSION: The antenatal prediction of lethality in this series of prenatal diagnosed skeletal dysplasias was correct. A correct antenatal diagnosis of the type of skeletal dysplasia was difficult, with 25 of 38 cases correctly diagnosed.
Assuntos
Amniocentese , Doenças do Desenvolvimento Ósseo/genética , Amostra da Vilosidade Coriônica , Aconselhamento Genético , Ultrassonografia Pré-Natal , Doenças do Desenvolvimento Ósseo/diagnóstico , Bases de Dados Genéticas , Feminino , Seguimentos , Humanos , Recém-Nascido , Gravidez , Segundo Trimestre da Gravidez , Terceiro Trimestre da Gravidez , Estudos Retrospectivos , SíndromeRESUMO
In the early 1990s Nicolaides introduced screening for trisomy 21 by fetal nuchal translucency thickness measurement with ultrasound between 11-13(+6) weeks. Already in 1866 L. Down noted that common features of patients with trisomy 21 are a skin being too large for the body and a flat face with a small nose. While detection rates for trisomy 21, given an invasive testing rate of 5%, were only 30% for screening by maternal age and 65% for screening by maternal serum triple test, the detection rate for screening by nuchal translucency combined with maternal age was 75% and this could be increased to 90% in combination with maternal serum screening (serum B-human chorionic gonadotropin and pregnancy-associated plasma protein-A) at 11-13(+6) weeks. The additional soft markers in the first trimester are the fetal nasal bone, the Doppler velocity waveform in the ductus venosus and tricuspid regurgitation and these markers can be used to further increase the detection rate of trisomy 21. In addition increased nuchal translucency thickness can also identify other chromosomal defects (mainly trisomy 13 and 18 and monosomy X) and major congenital malformations (mainly cardiac defects) and genetic syndromes.
Assuntos
Síndrome de Down/diagnóstico por imagem , Medição da Translucência Nucal , Transtornos Cromossômicos/ultraestrutura , Doenças em Gêmeos/diagnóstico por imagem , Doenças em Gêmeos/embriologia , Feminino , Humanos , Cariotipagem , Medição da Translucência Nucal/métodos , Valor Preditivo dos Testes , GravidezRESUMO
Subchorionic placental cysts occur in up to 5% of pregnancies. Large and numerous placental cysts increase the risk for intrauterine growth restriction. We describe a case with large multiple subchorionic placental cysts complicated by intracystic hemorraghe and fetal growth restriction.
RESUMO
OBJECTIVES: To investigate the natural history, associated abnormalities and outcome of 12 fetuses with arachnoid cyst diagnosed antenatally by ultrasound and magnetic resonance imaging and to compare the outcome with cases in the literature. METHODS: A retrospective study of all cases of antenatally detected fetal arachnoid cysts was performed in patients referred to a tertiary unit between 2007 and 2013. Associated abnormalities, pregnancy outcome and postnatal follow-up were analyzed. All papers about prenatally diagnosed arachnoid cysts, of the last 30 years, were evaluated (search terms in Pubmed: "prenatal diagnosis", "Arachnoid Cysts"). RESULTS: Fetal arachnoid cysts were diagnosed in 12 fetuses, 9 were females. The mean gestational age of diagnosis was 28 1/7 (range 19 1/7-34 2/7 weeks). A total of 9 cases were supratentorial, 3 were located in the posterior fossa. In 10 cases a fetal MRI was performed which confirmed brain compression in 4 out of 5 supratentorial arachnoid cyst. MRI did not reveal other malformations nor signs of nodular heterotopia. Only one fetus presented with additional major anomalies (bilateral ventricumomegaly of >20 mm and rhombencephalosynapsis) leading to a termination of pregnancy. Two neonates underwent endoscopic fenestration of the arachnoid cyst in the first week of life with no additional intervention in childhood. All but one (10/11) had a favorable postnatal outcome. This child suffered from visual impairment at autism was diagnosed at the age of 5. One child had a surgical correction of strabismus later in childhood. In one child the infratentorial arachnoid cyst regressed spontaneously on ultrasound and MRI in the postnatal period. CONCLUSIONS: The majority of arachnoid cysts in this series are of benign origin and remain stable. Based on the current series and the review of the literature, in the absence of other associated anomalies and when the karyotype is normal, the postnatal overall and neurological outcome is favorable. Large suprasellar arachnoid cysts however, may cause visual impairment and endocrinological disturbances. Rarely associated cerebral or cerebellar malformations are present. Modern postnatal management of suprasellar arachnoid cyst consists of endoscopic cystoventriculostomy.
Assuntos
Cistos Aracnóideos/patologia , Doenças Fetais/patologia , Anormalidades Múltiplas/epidemiologia , Cistos Aracnóideos/complicações , Feminino , Humanos , Masculino , Gravidez , Diagnóstico Pré-Natal , Estudos RetrospectivosRESUMO
We present further evidence for autosomal recessive inheritance of the bilateral tibial agenesis/ectrodactyly dysostosis. A consanguineous Turkish couple gave birth to three children with malformations. The first, a boy, died neonatally of pulmonary hypertension with congenital alveolar capillary dysplasia and also had tibial agenesis and ectrodactyly. A second child, a girl, died after birth with the same abnormality of the lungs without skeletal malformations. After the birth of three unaffected children, echographic examination at 15 weeks of gestation in the sixth pregnancy documented agenesis of tibiae and symmetrical ectrodactyly of hands and feet. Autopsy did not show additional malformations, and lung development was normal for gestational age. This observation also confirms the autosomal recessive inheritance pattern of congenital alveolar capillary dysplasia.
Assuntos
Deformidades Congênitas da Mão/patologia , Tíbia/anormalidades , Anormalidades Múltiplas/genética , Anormalidades Múltiplas/patologia , Adulto , Evolução Fatal , Feminino , Morte Fetal , Feto/anormalidades , Genes Recessivos/genética , Deformidades Congênitas da Mão/diagnóstico por imagem , Humanos , Tíbia/diagnóstico por imagem , Ultrassonografia Pré-NatalRESUMO
We report the second trimester prenatal diagnosis of severe symmetrical limb deficiencies with posterior fossa cyst and cardiac anomaly in a female fetus. Fetopathological examination revealed additional anomalies: renal-hepatic-pancreatic dysplasia, cleft palate, and Müllerian duct anomaly. The spectrum of congenital malformations in the present observation is difficult to classify into a single syndrome entity and presents an overlap with several syndromes: Roberts syndrome, Goldston syndrome, and renal-hepatic-pancreatic dysplasia.
Assuntos
Anormalidades Múltiplas/patologia , Fissura Palatina/patologia , Cistos/patologia , Cardiopatias Congênitas/patologia , Deformidades Congênitas dos Membros/patologia , Ductos Paramesonéfricos/anormalidades , Anormalidades Múltiplas/diagnóstico por imagem , Anormalidades Múltiplas/genética , Adulto , Fossa Craniana Posterior/patologia , Evolução Fatal , Feminino , Humanos , Cariotipagem , Rim/anormalidades , Fígado/anormalidades , Pâncreas/anormalidades , Gravidez , Segundo Trimestre da Gravidez , Síndrome , Ultrassonografia Pré-NatalRESUMO
We present a retrospective study of the frequency and type of associated malformations and chromosomal anomalies in 42 consecutive cases of congenital diaphragmatic hernia (CDH) diagnosed in utero during the period from 1985 to 1999. In 26% (11/42) of the cases, associated malformations were detected. Chromosomal anomalies were present in 9.5% (4/42). In this group of 15 cases (15/42 = 36%) with associated malformations or chromosomal anomalies, all cases, except one, had prenatal sonographic evidence of additional problems. The survival rate of fetuses with CDH and associated malformations or chromosomal anomalies was poor (1/15). Therefore, the overall survival rate of in utero-diagnosed CDH was only 31% (13/42), while isolated left CDH had a survival rate of 52% (12/23). The in utero diagnosis of CDH implies a detailed echographic examination to exclude additional anomalies. The risk for a syndromal or chromosomal malformation becomes small when no additional anomalies are seen on ultrasound.
Assuntos
Anormalidades Múltiplas/diagnóstico , Aberrações Cromossômicas , Hérnia Diafragmática/diagnóstico , Feminino , Hérnia Diafragmática/genética , Hérnias Diafragmáticas Congênitas , Humanos , Fígado/anormalidades , Mediastino/anormalidades , Poli-Hidrâmnios/etiologia , Gravidez , Resultado da Gravidez , Estudos Retrospectivos , Taxa de Sobrevida , Ultrassonografia Pré-NatalRESUMO
We report a 13-week-old female fetus with early onset fetal akinesia deformation sequence (FADS) and hydranencephaly. In a previous pregnancy, the same ultrasonographic findings were noted at 13 weeks. Fetopathological examination of both female fetuses confirmed FADS with severe arthogryposis, multiple pterygia, and muscular hypoplasia. Neuropathological examination showed massive cystic dilatation of the cerebral ventricles (hydranencephaly) with calcification of the basal ganglion and brain stem and a proliferative vasculopathy throughout the central nervous system. The findings in the two female siblings document the earliest echographic diagnosis of hydranencephaly, Fowler type, and this observation further supports autosomal recessive inheritance of this distinct type of hydranencephaly.
Assuntos
Artrogripose/genética , Doenças Fetais/genética , Hidranencefalia/genética , Doenças dos Gânglios da Base/genética , Tronco Encefálico/patologia , Malformações Vasculares do Sistema Nervoso Central/genética , Malformações Vasculares do Sistema Nervoso Central/patologia , Feminino , Doenças Fetais/diagnóstico por imagem , Feto , Genes Recessivos , Humanos , Hidranencefalia/diagnóstico por imagem , Núcleo Familiar , Síndrome , UltrassonografiaRESUMO
Objectives: It was the main aim of the present retrospective study carried out in Flanders to evaluate how women with a false-positive triple test result look back on their experience and decision making and how many of them make use of the triple test in subsequent pregnancies. Methods: All 508 women tested in the Centre for Human Genetics in Leuven in 1995 who had a positive triple test result followed by a normal amniocentesis outcome were invited to participate in a mailed questionnaire study with open and multiple choice questions in 1998. The response rate was 68%. Results: The answers to the multiple choice question assessing how they look back on their initial expectations regarding the exact meaning of the triple test revealed that less than one half reported that it concerned the identification of 'a higher risk of carrying a child with Down syndrome (DS)'. Reporting correct initial expectations was significantly associated with a higher education level. The same holds for indecisiveness regarding pregnancy termination should the amniocentesis have detected a fetus with DS. As expected, a large majority of the women reported a high level of distress or worry after the communication of the positive triple test result. Overall the findings show that retrospectively most women had the feeling that the decision to have amniocentesis was their own decision rather than a professional's. Of the subgroup with one or more subsequent pregnancies 70% had another triple test. Conclusions: The overall results of this study clearly reveal a need for a systematic approach aimed at better informing and counselling pregnant women about the implications and limitations of the triple test. Notwithstanding the reported high level of distress caused by a positive triple test result, a large majority of the women with subsequent pregnancies had another triple test; they represent a clearly higher percentage than in another recent study. Copyright 2001 S. Karger AG, Basel
RESUMO
Cytomegalovirus (CMV) is a frequent cause of congenital infections in humans occurring in 0.4 to 2.3% of life births. Although preexisting maternal antibodies are generally protective, transplacental transmission of CMV during pregnancy may occur after recurrent maternal infection. We report severe bilateral hearing loss in an infant affected as a result of a CMV reactivation in pregnancy.
Assuntos
Infecções por Citomegalovirus/complicações , Surdez/virologia , Complicações Infecciosas na Gravidez , Adulto , Surdez/etiologia , Feminino , Doenças Fetais/diagnóstico , Doenças Fetais/etiologia , Humanos , Recém-Nascido , Transmissão Vertical de Doenças Infecciosas , Espectroscopia de Ressonância Magnética , Gravidez , Ativação ViralRESUMO
Prenatal echographic diagnosis of laryngeal atresia as part of a multiple congenital anomalies (MCA) syndrome: In this report we present the prenatal second trimester echographic diagnosis of laryngeal atresia in a male fetus with multiple associated congenital anomalies: oesophageal atresia, crossed fused ectopy of the right kidney, mild cutaneous syndactyly of fingers III-V and toes II-III, distinct facial appearance and single umbilical artery. Bilateral voluminous echogenic lungs were the major echographic diagnostic sign. The associated multiple congenital anomalies were not diagnostic for a distinct, recognizable multiple malformation syndrome.
Assuntos
Anormalidades Múltiplas/diagnóstico por imagem , Anormalidades Múltiplas/genética , Doenças Fetais/diagnóstico por imagem , Doenças Fetais/genética , Laringe/anormalidades , Laringe/diagnóstico por imagem , Diagnóstico Pré-Natal , Adulto , Evolução Fatal , Feminino , Humanos , Masculino , Gravidez , Segundo Trimestre da Gravidez , Síndrome , UltrassonografiaRESUMO
We report first trimester cystic hygroma colli with subsequent resolution and development of a fetal akinesia deformation sequence. Neuropathological examination of the brain showed intra- and extracellular white matter edema while spinal cord, peripheral nerves and muscles were normal. Hygroma colli as the first echographic sign of subsequent severe fetal akinesia sequence without muscular dystrophy as seen in the Lethal Multiple Pterygium syndrome has not been previously reported.
Assuntos
Anormalidades Múltiplas/diagnóstico por imagem , Artrogripose/diagnóstico por imagem , Feto/anormalidades , Sistema Linfático/anormalidades , Linfocele/embriologia , Anormalidades Múltiplas/embriologia , Edema , Humanos , Sistema Linfático/diagnóstico por imagem , Sistema Linfático/embriologia , Linfocele/diagnóstico por imagem , Masculino , Ultrassonografia Pré-NatalAssuntos
Bradicardia , Síndrome de DiGeorge/diagnóstico , Anormalidades Musculoesqueléticas , Diagnóstico Pré-Natal , Amniocentese , Bradicardia/diagnóstico , Feminino , Humanos , Recém-Nascido , Masculino , Anormalidades Musculoesqueléticas/diagnóstico , Poli-Hidrâmnios , Gravidez , Ultrassonografia Pré-NatalRESUMO
In this report we describe a 17 weeks old female fetus with a lumbosacral meningocoele, multicystic renal dysplasia (Potter type IIb) and postaxial polydactyly type A at the left hand and left foot. There was no hepatic fibrosis. Although multicystic renal dysplasia and postaxial polydactyly are often present in the Meckel syndrome, a lumbosacral neural tube defect is not a typical finding in this syndrome.