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Skin health plays a crucial role in our overall well-being. It not only affects our physical
appearance but also impacts our self-confidence and mental health. While many factors
contribute to the health and appearance of our skin, one key aspect that often gets
overlooked is genetics. Genetics can play a significant role in determining the
characteristics and conditions of our skin.
Certain skin conditions have a strong genetic
component. For example, conditions like eczema, psoriasis, and acne have been
linked to specific genetic variations. If you have a family history of these conditions,
you may have an increased likelihood of developing them as well.
Additionally, conditions like skin cancer, melasma, and vitiligo can also be influenced
by genetics. By identifying genetic markers associated with these conditions, medical
professionals can provide early detection, prevention strategies, and personalized
treatment plans tailored to your genetic predispositions.
Individuals with any conditions like eczema, psoriasis, and acne that have been linked
to specific genetic variations.
If you have a family history of genetic conditions, you may have an increased
likelihood of developing them as well such as: Albinism, Birthmarks, Carney complex,
Cowden syndrome, Dyskeratosis congenita, Ectodermal dysplasia, Focal dermal
hypoplasia (Goltz-Gorlin syndrome, Hemangioma,…..etc. .
The treatment of people who have hereditary dermatologic conditions requires accurate
diagnosis. Dermatologists understand how these conditions can affect your skin,
including whether they relate to any other condition or disease.
They evaluate skin pigmentation and skin discoloration disorders and other disorders, before they can recommend best diseases management to treat or reduce complications of your skin conditions.
Scroll to bottom of page to learn more about each Dermatology Testing.
Please reach us at contact@genatechs.com to order your panel or if you cannot find test needed.
CDH3, DLX3, EDA, EDAR, EDARADD, EVC, EVC2, GJB6, GRHL2, HOXC13, KDF1, KREMEN1, KRT74, KRT85, MBTPS2, MSX1, NFKBIA, NLRP1, ORAI1, PKP1, PVRL1, PVRL4, TP63, TWIST2, WNT10A
CD151, COL17A1, COL7A1, DSP, DST, EXPH5, FERMT1, ITGA3, ITGA6, ITGB4, KRT14, KRT5, LAMA3, LAMB3, LAMC2, MMP1, PKP1, PLEC, TGM5
ABCA12, ABHD5, ALDH3A2, ALOX12B, ALOXE3, AP1S1, CASP14, CDSN, CERS3, CLDN1, CSTA, CYP4F22, DSG1, DSP, EBP, FLG, GJB2, GJB3, GJB4, KRT1, KRT10, KRT2, LIPN, LOR, NIPAL4, PHGDH, PHYH, PNPLA1, POMP, PSAT1, SLC27A4, SLURP1, SNAP29, SPINK5, ST14, STS, TGM1, TGM5
C10orf11, MC1R, OCA2, SLC24A5, SLC45A2, TYR, TYRP1
Single Gene
DDB2, ERCC2, ERCC3, ERCC4, ERCC5, POLH, XPA, XPC
Single Gene
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Single Gene
Single Gene
Single Gene
Single Gene
Single Gene
Single Gene
Single Gene
Single Gene
Single Gene
Single Gene
Single Gene
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