HeLab Medical Center Analysis
It is a laboratory specialized in male and female urogenital microbiological analyses.
Our analyzes are specific for:
- Pregnancy research and PMA paths (medically assisted procreation)
- Sexually transmitted infection (STI) screening
- Prevention for women
- Prevention for men
- Pregnancy test urine delivery or blood sampling (Beta Hcg dosage).
- Single and couple Karyotype and Cystic Fibrosis 152 mutations. Book here.
- Bacterioscopic examination
- Chlamydia and Gonorrhea from urine 1° void (PCR Method)
- Chlamydia/Gonorrhea from endocervical swab (PCR method)
- Endourethral swab
- Endourethral swab with sexually transmitted diseases (PCR method)
- Endourethral swab with sexually trasmitted diseases (PCR method)
- Herpes test 1/2
- Herpes Zooster test
- HPV screening – HPV typed
- Lesion swab
- Oropharyngeal swab
- Urine 1° void
- Urine 1° void with sexually trasmitted diseases (PCR method)
- Urine culture
- Vaginal pH evaluation
- Vaginal swab
- Vaginal swab
- Vaginal swab searching mycoplasmas and ureaplasmas
- Vaginal-endocervical swab with sexually tramitted diseases (PCR method)
- Vagino-rectal pregnancy swab
- Vulvar swab
- Chlamydia and Gonorrhea from urine 1° void (PCR Method)
- Chlamydia/Gonorrhea from endourethral swab (PCR Method)
- Endourethral swab
- Endourethral swab
- Endourethral swab with sexually transmitted diseases (PCR method)
- Glans swab
- Glans swab
- Herpes 1/2
- Herpes Zooster test
- HPV screening – HPV typed
- Lesion swab
- Oropharyngeal swab
- Oropharyngeal swab for streptococcus
- Spermioculture
- Spermioculture with sexually trasmitted diseases (PCR Method)
- Urine 1° void
- Urine 1° void with sexually trasmitted diseases (PCR method)
- Urine culture
- 21 Hydroxylase – deficiency
- ACE
- APO B
- APO E
- BCRA1
- BCRA1+2
- BCRA2
- Beta Fibrinogen
- Beta Thalassemia
- Congenital deafness – whole coding region – GENE GJB2 (code CX26)
- Congenital deafness – entire coding region – GENE GJB2 (code CX26)
- Couple karyotype on peripheral blood
- Cystic Fibrosis (152 MUTATIONS)
- Factor II (prothrombin G20210A)
- FSHR gene (for FSH receptor)
- Hemochromatosis (3 mutations) – HFE (C282Y,S65C,H63D)
- HLA-G
- Karyotype on peripheral blood
- LEIDEN FACTOR V
- MHL1 – gene sequence analysis
- Microdeletion of the Y chromosome
- MTHFR MUTATION C677T
- MYOTONIC DYSTROPHY-SI STEINERT DISEASE (MPK)
- PAI 1
- Panel 4 mutations (factor V, II, MTHFR C677T A1298C)
- Panel 5 mutations (Factor V Leiden, V Cambridge, Y1702C, H1299R, Factor II)
- Spinal muscular atrophy – SMA (SMA1)
- X-FRAGILE FRAXA
- X-FRAGILE FRAXE
- Y chromosome microdeletion
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Request a quote for your analyzes by sending an email to info@helabflorence.com or calling 055 474983
- The staff speaks English
- Booking of home health services on request (blood sampling, genetic tests, Covid tests)
- Samples delivery and reports collection:
Florence, Helab from Monday to Friday 8:30 – 18:30 without appointment; - English translation of the Covid report with tipe and number of travel document
