TITLE

Letter: Vaginal cytology in pregnancies associated with congenital fetal defects

AUTHOR(S)
Sen, D K
PUB. DATE
May 1974
SOURCE
British Medical Journal;5/4/1974, Vol. 2 Issue 5913, p277
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
No abstract available.
ACCESSION #
64110318

 

Related Articles

  • Congenital Malformations and ART: Risks and Implications for Prenatal Diagnosis and Fetal Medicine. Hobbins, John C. // OB/GYN Clinical Alert;May2010, Vol. 26 Issue 13, p1 

    The article discusses the congenital malformations in pregnancies conceived through assisted reproductive technology (ART). It states that children born after ART show higher rate of major congenital complications. The recent Swedish registry study indicates that 16,000 ART children showed a 42%...

  • Diagnóstico antenatal de malformação adenomatoide cística congênita unilateral associada à síndrome de Taussig-Bing: relato de caso. Mombaque dos Santos, Caroline; Mombaque dos Santos, Wendel; Pigatto, Camila; Feltrin, Marcelo; dos Santos, Larissa Fonseca; Pancich Gallarreta, Francisco Maximiliano // Scientia Medica;jul-set2014, Vol. 24 Issue 3, p10 

    AIMS: To report a rare case of antenatal diagnosis of unilateral congenital cystic adenomatoid malformation associated with Taussig-Bing syndrome. CASE DESCRIPTION: Patient aged 40 years, four pregnancies with three previous vaginal deliveries, black skin, married, housewife, without prior...

  • Fetal Outcomes Associated With Metoclopramide Use in Pregnancy. Vrachnis, Nikolaos; Zygouris, Dimitrios; Iliodromiti, Zoe // JAMA: Journal of the American Medical Association;2/12/2014, Vol. 311 Issue 6, p623 

    A letter to the editor is presented in response to the article "Metoclopramide in Pregnancy and Risk of Major Congenital Malformations and Fetal Death" by B. Pasternak and colleagues in the 2013 issue.

  • VAGINAL DELIVERY IN A PATIENT OF EISENMENGER SYNDROME. KALRA, PRIYANKA // Indian Journal of Medical Sciences;Nov/Dec2012, Vol. 66 Issue 11/12, p289 

    Eisenmenger syndrome consists of a congenital communication between the systemic and pulmonary circulation, with resultant pulmonary arterial hypertension and reversal of flow through the defect. Pregnancy in the setting of pulmonary hypertension and Eisenmenger physiology is associated with a...

  • Prenatally diagnosed fetal omphalocele at 11 week gestation - a case report. Protrka, Zoran; Dimitrijevic, Aleksandra; Kastratovic, Tatjana; Djuric, Janko; Arsenijevic, Petar; Novakovic, Tanja; Milosavljevic, Milos // Central European Journal of Medicine;Aug2013, Vol. 8 Issue 4, p431 

    Omphalocele is the most common congenital defect of the abdominal wall and in a large percentage of cases it is associated with chromosomal anomalies. In this case report during the regular ultrasound examination at 11 weeks of gestation, omphalocela, whose scope was 90% of fetal abdomen, was...

  • Residential Mobility during Pregnancy for Mothers of Infants with or without Congenital Cardiac Anomalies. Shaw, Gary M.; Malcoe, Lorraine Halinka // Archives of Environmental Health;Sep/Oct91, Vol. 46 Issue 5 

    Focuses on the impact of residential mobility on the first trimester of pregnancy in California. Effect of parental employment on pregnancy; Assumption on the fetal exposure to environmental agents; Association between maternal environmental exposure and congenital malformations.

  • First trimester diagnosis of VACTERL association. Santos, Joana; Nogueira, Rosete; Pinto, Rita; Cerveira, Isabel; Pereira, Susana // Clinics & Practice;2013, Vol. 3 Issue 1, p11 

    VACTERL association (OMIM 192350) is a non-random combination of multiple congenital malformations including vertebral, anal, cardiac, tracheoesophageal, renal and limb anomalies. The wide spectrum of defects suggests the occurrence of defective development during early embryogenesis. The...

  • Alobar holoprosencephaly: a case report. Kurtulmuş, Seçil Karaca; Ekmekçi, Emre; Aydoğmuş, Serpil; Yıldırım, Alkım; Kelekçi, Sefa // Perinatal Journal / Perinatoloji Dergisi;Oct2014 Supplement, Vol. 22, pSE16 

    Alobar holoprosencephaly is a rare and severe congenital brain anomaly which is caused by developmental defect in the fore brain associated with non-disjunction of both hemispheres and ventricles during embryonic period. Depending on the severity of non-disjunction, holoprosencephaly can be...

  • Ectopia cordis: a case report. Mesquita Dias, Gonçalo Filipe Infante; dos Reis Santos, Ana Vanessa; Paixão Martins, Cátia Filipa Cabrita; Duarte Ferreira, Ana Paula; da Fonseca, Joaquim Marques Dinis // Revista Brasileira de Saude Materno Infantil;jul-set2014, Vol. 14 Issue 3, p287 

    Introduction: ectopia cordis is a rare congenital malformation, with an estimated incidence of 5 to 8 per million live births. It is defined as a malformation in which the heart is located in an extra-thoracic position. Ectopia cordis may occur as an isolated malformation or associated with...

  • The Effect on the Fetus of Medications Used to Treat Pregnant Inflammatory Bowel-Disease Patients. Moskovitz, David Norman; Bodian, Carol; Chapman, Mark L.; Marion, James F.; Rubin, Peter H.; Scherl, Ellen; Present, Daniel H. // American Journal of Gastroenterology;Apr2004, Vol. 99 Issue 4, p656 

    OBJECTIVES: We reviewed data to investigate the effect of 5-ASA drugs, metronidazole, ciprofloxacin, prednisone, 6-mercaptopurine, azathioprine, and cyclosporine on pregnancy outcomes in patients with inflammatory bowel disease (IBD).METHODS: One hundred and thirteen female patients with a total...

Share

Read the Article

Other Topics