Journal Basic Info

  • Impact Factor: 1.809**
  • H-Index: 6
  • ISSN: 2474-1655
  • DOI: 10.25107/2474-1655
**Impact Factor calculated based on Google Scholar Citations. Please contact us for any more details.

Major Scope

  •  Emergency Medicine and Critical Care
  •  Depression
  •  Tuberculosis
  •  Vascular Medicine
  •  Asthma
  •  Hepatology
  •  Renal Disease
  •  Cardiology

Abstract

Citation: Ann Clin Case Rep. 2022;7(1):2120.DOI: 10.25107/2474-1655.2120

Predictive Factors for Pregnancy Termination Following a Prenatal Diagnosis of Down Syndrome: Experience from the Reunion Registry of Congenital Malformations from 2002 to 2015

Léa Bruneau1,2,3*, Victorine Lenclume1,2, Nicolas Iv3, Catherine Marimoutou2,3, Bénédicte Bertaut-Nativel1 and Hanitra Randrianaivo1

1The Reunion Registry of Congenital Malformations REMACOR, France 2INSERM CIC 1410 Clinical and Epidemiology, University Hospital, France 3Department of Public Health and Research Support, Methodological Support and Biostatistics Unit, University Hospital, France

*Correspondance to: Léa Bruneau 

 PDF  Full Text Short Communication | Open Access

Abstract:

#

Keywords:

Cite the Article:

Bruneau L, Lenclume V, Iv N, Marimoutou C, Bertaut-Nativel B, Randrianaivo H. Predictive Factors for Pregnancy Termination Following a Prenatal Diagnosis of Down Syndrome: Experience from the Reunion Registry of Congenital Malformations from 2002 to 2015. Ann Clin Case Rep. 2022; 7: 2120..

Search Our Journal

Journal Indexed In

Articles in PubMed

Does Autoimmunity have a Role in Myoclonic Astatic Epilepsy? A Case Report of Voltage Gated Potassium Channel Mediated Seizures
 PubMed  PMC  PDF  Full Text
A New Minimally Invasive Procedure for Muscle, Back, Neck Pain and Radiculopathy - The Myofascial Nerve Block
 PubMed  PMC  PDF  Full Text
View More...

Articles with Grants

Thyroid Hormone Resistance Syndrome Caused by Heterozygous R338W Mutation in Thyroid Hormone Receptor β: Report of one Chinese Pedigree a in Southwest China
 Abstract  PDF  Full Text
Detailed Phenotype Characterization of a Patient with a Novel Mutation in the SPAST Gene
 Abstract  PDF  Full Text
View More...