The amount of dermal filler needed is decided by the practitioner during the consultation.
Consultation £180
(Redeemable against treatment)
The most commonly requested areas are Frown, Forehead & Crows Feet
Prices include a review at two weeks, and if required, and adjustment treatment at that time. We do not charge a supplement for men, nor for higher dosage needs.
Includes 90% Oxygen mask
Cleansing, exfoliation, facial massage, mask
Cleansing, exfoliation, facial massage, mask, serum, deep hydradermabrasion with ultrasound
Cleansing, mask, serum
Cleansing, mask, serum, LED light therapy
Cleansing, exfoliation, lifting facial massage, mask
Cleansing, exfoliation, lifting facial massage, mask, serum, RF treatment
Deep cleansing, enzyme therapy, mask
Deep cleansing, enzyme therapy, mask, serum, LED light treatment
Mask and collagen patch
Enzyme therapy, massage, and mask
1. Breast cancer 2. Lung cancer (including bronchus) 3. Prostate cancer 4. Colorectal cancer (colon and rectal) 5. Melanoma (skin cancer) 6. Bladder cancer 7. Non-Hodgkin's lymphoma 8. Kidney cancer (renal cell and renal pelvis) 9. Endometrial cancer (uterine) 10. Leukemia 11. Pancreatic cancer 12. Thyroid cancer This test helps identify individuals who may benefit from enhanced screening or preventive measures, allowing for early detection and intervention.
Analyses the entire coding region of DNA to detect mutations in genes linked to hereditary cancer syndromes. This thorough assessment provides a comprehensive view of genetic cancer risk, enabling personalised prevention strategies.
**Predisposition Risk Scoring (15+ conditions):** Assesses genetic risk factors for multiple common hereditary diseases, such as heart disease, diabetes, and certain cancers. This test allows for early intervention and lifestyle modifications, potentially preventing or delaying disease onset.
**Diagnostic Exome:** Examines all protein-coding genes in the genome to identify genetic variants causing rare inherited disorders. This test is particularly useful for diagnosing complex or undiagnosed genetic conditions, offering insights into rare diseases.
Uses comparative genomic hybridisation to detect chromosomal abnormalities, including deletions and duplications, associated with autism spectrum disorders. This test helps identify specific genetic causes of autism, aiding in diagnosis and treatment planning.
Provides a comprehensive analysis of all protein-coding genes to identify mutations associated with autism spectrum disorders. This test offers a deeper understanding of the genetic factors contributing to autism, potentially leading to more targeted interventions.
**Comprehensive Carrier Screening (400+ conditions including Cystic Fibrosis, GJB2, etc.):** Tests for genetic mutations that could be passed on to children, including those causing cystic fibrosis, GJB2-related hearing loss, and Tay-Sachs disease. This screening is essential for family planning, allowing couples to make informed decisions about reproduction.
Analyses genetic variations that influence how an individual metabolises and responds to different medications. This test helps healthcare providers optimise drug selection and dosing, reducing adverse effects and improving treatment efficacy. It is particularly useful for tailoring treatments in various medical fields.
These tests collectively offer a comprehensive approach to genetic health assessment, from cancer prevention to personalised medication management, providing valuable insights for individuals and healthcare providers alike.
2 North Terrace, South Kensington, London SW3 2BA