SCREENING STI (Sexually Transmitted Infectious)
- Infectious blood test (STI blood tests)
- Swabs or Urine 1° void in PCR + Blood test for Chlamydia antibodies (STI)
- Swabs or Urine 1° void in PCR + Blood test for Herpes 1-2 antibodies (STI)
- Swabs or Urine 1° void in PCR + Blood test Hepatitis B and C (STI)
- Swabs or Urine 1° void in PCR + Infectious blood tests package (STI)
- Swabs or Urine 1° void in PCR + Screening HIV and SYPHILIS (STI)
FEMALE TESTS
- Bacterioscopic examination
- Chlamydia and Gonorrhea from urine 1° void (PCR Method)
- Chlamydia/Gonorrhea from endocervical swab (PCR method)
- Chlamydia/Gonorrhea from endourethral swab (PCR Method)
- Endourethral swab
- Endourethral swab with sexually transmitted diseases (PCR method)
- Herpes test 1/2
- Herpes Zooster test
- HPV screening – HPV typed
- Lesion swab
- Oropharyngeal swab for streptococcus
- Oropharyngeal swab in PCR
- 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
MALE TESTS
- Chlamydia and Gonorrhea from urine 1° void (PCR Method)
- Chlamydia/Gonorrhea from endourethral swab (PCR Method)
- Endourethral swab
- Endourethral swab with sexually transmitted diseases (PCR method)
- Glans swab
- Herpes 1/2
- Herpes Zooster test
- HPV screening – HPV typed
- Lesion swab
- Oropharyngeal swab for streptococcus
- Oropharyngeal swab in PCR
- Sperm culture
- Sperm culture with sexually transmitted diseases (PCR Method)
- Urine 1° void
- Urine 1° void with sexually trasmitted diseases (PCR method)
- Urine culture
GENETIC
- 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/A1298C
- 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
