Mycoplasma genitalium

Mycoplasma genitalium testing is a molecular diagnostic service that detects M. genitalium DNA using sensitive nucleic acid amplification tests (NAAT/PCR) from first‑catch urine or genital swabs. Some assays also identify macrolide‑resistance associated 23S rRNA mutations to guide targeted antibiotic therapy. Accurate identification of the organism and resistance markers is important because M. genitalium is a frequent cause of non‑gonococcal urethritis in men and can cause cervicitis, pelvic inflammatory disease and contribute to infertility in women.

This home testing option provides discreet sample collection with analysis performed by UAE‑certified laboratories and rapid electronic reporting to support timely clinical decisions and treatment. It is recommended for symptomatic individuals (dysuria, abnormal discharge, pelvic pain), those with persistent or recurrent urethritis after treatment, sexual partners of confirmed cases, or anyone with recent unprotected exposure who seeks peace of mind; always review results with a healthcare professional for appropriate management in the UAE context.

• Mycoplasma genitalium DNA (NAAT/PCR)
• Macrolide‑resistance mutations (23S rRNA)
• Sample adequacy / internal control

• Urethral or vaginal discharge, burning or pain on urination
• Persistent or recurrent symptoms after prior STI treatment
• Recent unprotected sex or exposure to a partner with an STI
• Pelvic pain, cervicitis, or suspected pelvic inflammatory disease
• Part of infertility workup when clinically indicated

• Discreet at‑home sample collection with certified UAE laboratory processing
• High‑sensitivity NAAT for accurate detection of M. genitalium
• Optional macrolide‑resistance testing to guide effective antibiotic choice
• Fast electronic reporting to support timely treatment decisions
• Confidential results and linkage to local clinical care if needed

• First‑catch urine sample: avoid urinating for at least 1 hour before collection
• For vaginal testing: self‑collected vaginal swab (follow kit instructions) or clinician swab
• Avoid sexual intercourse, douching or intravaginal products for 24 hours before sampling
• Valid Emirates ID and consent; testing for adults (follow UAE guidance for minors and parental consent)