Fetal abnormalities testing in Scandriglia

Find health labs to test for Fetal abnormalities in Scandriglia and compare all offers by prices and services.

Tests that cover Fetal abnormalities

Cytologic Examination
Esame citologico urinario con autoprelievo by innovabiohealth S.r.l.

Test at-Home / Self-testing

Featured

€70.00

€66.50 with our promocode

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Cytology Test by Laboratorio Sabino Srl

Via Servilia, 12, 02032 Fara in Sabina RI, Italia

6.5 km

Unverified

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Cytology Test by Analisi Cliniche Ciocci Srl

Via Palatina, 00019 Tivoli RM, Italia

14.1 km

Unverified

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Cytology Test by Laboratorio analisi cliniche e microbiologiche Santa Croce Srl

Viale Niccolò Arnaldi, 15, 00019 Tivoli RM, Italia

14.1 km

Unverified

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Cytology Test by Centro Raphael

Via Mattè Trucco, 00132 Roma RM, Italia

26.3 km

Unverified

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TCT Test by Eurofins Genoma

Via di Castel Giubileo, 11, 00138 Roma RM, Italia

26.3 km

Unverified

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Cytology Test by Centro Ricerche Cliniche Ortasa S.r.l.

Via San Leo, 30, 00138 Roma RM, Italia

26.3 km

Unverified

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TCT Test by Unione Sanitaria Internazionale Spa

Via Gaspare Pacchiarotti, 95, 00139 Roma RM, Italia

26.3 km

Unverified

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Cytology Test by Studio Polispecialistico Nomentano

Via Nomentana, 550, 00141 Roma RM, Italia

26.3 km

Unverified

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TCT Test by Laboratorio Analisi Cliniche Tiburtino

Viale Fernando Santi, 38, 00155 Roma RM, Italia

26.3 km

Unverified

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TCT Test by Unione Sanitaria Internazionale Spa

Via dei Durantini, 360, 00157 Roma RM, Italia

26.3 km

Unverified

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Fetal abnormalities - symptoms and how to test

An abnormality in fetal development is called a fetal anomaly if it occurs during the first trimester of pregnancy. Between 2 and 3% of pregnant women may be told their unborn child has a fetal anomaly, often known as a congenital disability. Congenital disabilities and congenital abnormalities are other names for fetal abnormalities. Many fetal abnormalities have a genetic component, and prenatal screening tests can help parents determine the likelihood that their child will be born with one of these conditions. The tests include blood tests, a specific type of ultrasound and prenatal cell-free DNA screening.