Raskauden ajan ultraäänitutkimukset ja seerumiseulonnat rakenne- ja kromosomipoikkeavuuksien tunnistamisessa (FinOHTAn raportti 27/2005)

Publication Details

English Translation:

Maternal ultrasound and serum screening in the detection of structural and chromosomal abnormalities

Author(s):

• FinOHTA (FI) - Finnish Office for Health Care Technology Assessment

Country(ies) of application:

• Finland

Language(s):

• English
• Finnish

Type of Publication:

Evidence report

Publication URL:

Open Publication URL in a new window

Publication Scope:

• Assessment/diagnosis

Publication Status:

Published

Date of publication:

Aug 01, 2005

Due for Review:

-

Diseases / Conditions Addressed

MeSH Terms addressed:

• Congenital, Hereditary, and Neonatal Diseases and Abnormalities (C16)
  • Infant, Newborn, Diseases (C16.614)
  • Genetic Diseases, Inborn (C16.320)
  • Abnormalities (C16.131)
• Diagnosis (E01)
  • Diagnostic Techniques and Procedures (E01.370)
    • Diagnostic Imaging (E01.370.350)
• Female Genital Diseases and Pregnancy Complications (C13)
  • Pregnancy Complications (C13.703)
• Public Health (N06.850)
  • Public Health Practice (N06.850.780)
    • Mass Screening (N06.850.780.500)

Guideline key questions