Your Partner in Health and Wellness
Location
Head Office: Wellcare Health Clinic, Nazım Hikmet Caddesi, Omağ Sitesi, Blok F1, Dükkan 3, Aydemet Metehan, Lefkoşa Nicosia Branch: Miracle Hastanesi, Prof. Hilmi İleri Sokak No:24, Lefkoşa, Kıbrıs Kyrenia Branch: Medicalport Tunççevik Hastanesi, Kurtuluş Caddesi, Numara 70, Bellapais Yolu, Girne, Kıbrıs
PrenatalSafe® Test Options
OUR TEST OPTIONS:
Our broad portfolio, so that you can choose the most suitable screening test, is as follows: Always consult your doctor before deciding which test is right for you.
PrenatalSafe5
- Screens for aneuploidies of chromosomes 21, 18, 13 and the sex chromosomes (X and Y)
- Determination of fetal sex
PrenatalSafe5 + DiGeorge
- Screens for aneuploidies of chromosomes 21, 18, 13 and the sex chromosomes (X and Y)
- Determination of fetal sex
- Screens for DiGeorge syndrome microdeletion
PrenatalSafePlus
- Screens for aneuploidies of chromosomes 21, 18, 13, 9, 16 and the sex chromosomes (X and Y)
- Determination of fetal sex
- Screens for microdeletions of DiGeorge syndrome, 1P36 deletion syndrome, Angelman syndrome, Prader-Willi syndrome, Cri-Du-Chat syndrome, Wolf-Hirschhorn syndrome
Ninalia
- Screens for aneuploidies of all chromosomes, including the sex chromosomes
- Determination of fetal sex
PrenatalSafeKaryo Plus
- Screens for aneuploidies of all chromosomes, including the sex chromosomes
- Determination of fetal sex
- Screens for microdeletions of DiGeorge syndrome, 1P36 deletion syndrome, Angelman syndrome, Prader-Willi syndrome, Cri-Du-Chat syndrome, Wolf-Hirschhorn syndrome, Jacobsen syndrome, Langer-Giedion syndrome and Smith-Magenis syndrome
PrenatalSafeComplete Plus
- Screens for aneuploidies of all chromosomes, including the sex chromosomes
- Determination of fetal sex
- Screens for microdeletions of DiGeorge syndrome, 1P36 deletion syndrome, Angelman syndrome, Prader-Willi syndrome, Cri-Du-Chat syndrome, Wolf-Hirschhorn syndrome, Jacobsen syndrome, Langer-Giedion syndrome and Smith-Magenis syndrome
- Screens the fetus for single-gene diseases with GeneSafe
PrenatalSafeFull Risk
- Screens for aneuploidies of all chromosomes, including the sex chromosomes
- Determination of fetal sex
- Screens for microdeletions of DiGeorge syndrome, 1P36 deletion syndrome, Angelman syndrome, Prader-Willi syndrome, Cri-Du-Chat syndrome, Wolf-Hirschhorn syndrome, Jacobsen syndrome, Langer-Giedion syndrome and Smith-Magenis syndrome
- Screens the fetus for single-gene diseases with GeneSafe
- Performs carrier disease screening in the parents with GeneScreen