scholarly journals VP10.19: Outcome of prenatal diagnosis of club foot: a single institution experience

2021 ◽  
Vol 58 (S1) ◽  
pp. 135-135
Author(s):  
W. Abdallah ◽  
M. Nassar
Keyword(s):  
Prenatal Diagnosis ◽  
Club Foot ◽  
Single Institution

scholarly journals Frequencies of Fetal Chromosomal Abnormalities at Prenatal Diagnosis: 10 years experiences in a single institution

2001 ◽  
Vol 16 (3) ◽  
pp. 290 ◽  
Author(s):  
So Yeon Park ◽  
Jin Woo Kim ◽  
Young Mi Kim ◽  
Jin Mee Kim ◽  
Moon Hee Lee ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Chromosomal Abnormalities ◽  
Single Institution

scholarly journals OC235: Prenatal diagnosis of skeletal dysplasias in a single institution

2007 ◽  
Vol 30 (4) ◽  
pp. 439-439 ◽  
Author(s):  
T. Schramm ◽  
B. Tutschek ◽  
S. Minderer ◽  
C. Daumer-Haas ◽  
K. Hörtnagel ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Single Institution ◽  
Skeletal Dysplasias

Prenatal diagnosis and clinical significance of cephalocele—A single institution experience and literature review

2020 ◽  
Vol 40 (5) ◽  
pp. 612-617
Author(s):  
Sylwia Dąbkowska ◽  
Anna Kucińska‐Chahwan ◽  
Anna Beneturska ◽  
Alicja Ilnicka ◽  
Beata Nowakowska ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Literature Review ◽  
Clinical Significance ◽  
Single Institution

scholarly journals Prenatal Diagnosis of Chromosome 22q11.2 Deletions: Experiences in a Single Institution

2013 ◽  
Vol 10 (2) ◽  
pp. 99-103
Author(s):  
Yong Hwa Chae ◽  
Dong Wook Kwak ◽  
Moon Young Kim ◽  
So Yeon Park ◽  
Bom Yi Lee ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Single Institution ◽  
Chromosome 22Q11.2

scholarly journals Outcome of prenatal diagnosis of clubfoot: a single institution experience

2021 ◽  
Author(s):  
Wael Abdallah ◽  
Malek Nassar
Keyword(s):  
Risk Factors ◽  
Prenatal Diagnosis ◽  
Significant Relationship ◽  
Antenatal Diagnosis ◽  
False Positive Rate ◽  
Multiple Pregnancies ◽  
Single Institution ◽  
Maternal Characteristics ◽  
Live Births ◽  
Positive Rate

Aim: To assess the accuracy of antenatal diagnosis of clubfoot (CF), risk factors and outcomes in postnatal. Patients & methods: Maternal characteristics, sonographic signs and postnatal outcomes were evaluated in 60 patients with a prenatal diagnosis of CF between 2007 and 2020. Results: The rate of antenatal diagnosis of CF was 3.72/1000 live births. The false-positive rate was 6.67%. 66.7% of fetuses had bilateral CF and 33.3% had unilateral CF; 58.3% were isolated and 41.7% were complex; 58.3% were males and 41.7% were female; 16.7% were multiple pregnancies and 10% were cases of consanguinity. Conclusion: The accuracy of the diagnosis of CF depends on the operator’s skills. A significant relationship is demonstrated between the interruption of pregnancy, consanguinity, laterality and complexity.

Prenatal diagnosis and successful initial closure in classic bladder exstrophy: a single institution experience

2015 ◽  
Vol 221 (4) ◽  
pp. e147-e148
Author(s):  
Christopher A. Hesh ◽  
Pokket Sirisreetreerux ◽  
Ezekiel Young ◽  
Heather Di Carlo ◽  
John Gearhart
Keyword(s):  
Prenatal Diagnosis ◽  
Bladder Exstrophy ◽  
Single Institution

scholarly journals Prenatal Invasive Testing: A 4-Years Single Institution Experience in Turkey

2016 ◽  
Vol 21 (3) ◽  
Author(s):  
Emre Ekmekçi ◽  
Kutlu Kurt ◽  
Servet Gençdal ◽  
Emine Demirel ◽  
Sefa Kelekçi
Keyword(s):  
Prenatal Diagnosis ◽  
Invasive Procedures ◽  
Single Institution ◽  
Abnormal Karyotype ◽  
Non Invasive ◽  
Prenatal Diagnostic ◽  
Ultrasound Findings ◽  
Demographic Distribution ◽  
Fetal Karyotype

<p><strong>OBJECTIVE:</strong> Evaluation of indications, methods and results of prenatal diagnostic invasive procedures performed in our clinic in a four-year process and interpretation of relations between them.</p><p><strong>STUDY DESIGN:</strong> In this study 553 patients were examined retrospectively, who were undergone prenatal invasive procedures in our clinic for determination of fetal karyotype. Demographic distribution of the patients, indications for tests and results were examined, complications were evaluated depending on the procedure.</p><p><strong>RESULTS:</strong> A total of 41 abnormal karyotype pregnancies detected, the most common abnormal karyotype was trisomy 21 and most of abnormal karyotypes were detected in patients who undergone invasive diagnostic tests due to abnormal ultrasound findings. Abortion is resulted at two patients.</p><p><strong>CONCLUSION:</strong> Although non-invasive prenatal diagnosis is more accessible today and has become more preferable, prenatal invasive diagnosing still remains its importance in prenatal diagnosis. Especially in the cases with presence of abnormal ultrasound findings, invasive prenatal diagnosis should be the primary diagnostic method.</p>

A new strategy for prenatal diagnosis in a sporadic haemophilia B family

Haemophilia ◽  
2001 ◽  
Vol 7 (4) ◽  
pp. 416-418 ◽  
Author(s):  
M. Acquila ◽  
F. Bottini ◽  
A. Valetto ◽  
D. Caprino ◽  
P. G. Mori ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Haemophilia B ◽  
New Strategy
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