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Medical conditions related to the ear, nose or throat. They can include issues like hearing loss, sinusitis, throat infections and even allergies. While these conditions are incredibly common, the reasons why some people get them more frequently than others can sometimes be attributed to their genetic makeup.
Genes play an important role in congenital hearing loss, causing about 60 percent deafness in infants. One of the most common congenital (present at birth) abnormalities is hearing loss or deafness, affecting as many as three of every 1,000 babies. Exact data is not available, but it is likely that genes also play an important role in hearing loss in the elderly.
There are many genetic body Syndromes where patients have different levels of hearing
loss. About 15-30% of hearing loss cases passing down from parents are syndromic. Over
400 syndromes are known to include hearing loss. They can be caused by chromosomes
that are not normal (having extra or missing chromosomes, or parts of chromosomes),
parents passing them to children, or due to many factors working together, including
genetic and environmental.
Here’s some common disorders where genetic testing might of help in diagnosis:
Understanding your family history can be extremely beneficial in managing ENT disorders. When you know which conditions are prevalent in your family, you can take proactive steps to monitor symptoms and seek early treatment.
While you can’t change your genes, you can adopt lifestyle changes to manage or reduce the severity of ENT disorders. This might include avoiding allergens, using air purifiers at home and maintaining good hygiene practices to prevent infections.
Please reach us at contact@genatechs.com if you cannot find an answer to your question.
ACTB, ACTG1, ADCY1, ADGRV1, AIFM1, ATP6V1B1, BCS1L, BDP1, BSND, BTD,
CABP2, CACNA1D, CCDC50, CD164, CDC14A, CDH23, CEACAM16, CIB2, CISD2,
CLDN14, CLIC5, CLPP, CLRN1, COCH, COL11A1, COL11A2, COL2A1, COL4A3,
COL4A4, COL4A5, COL4A6, COL9A1, COL9A2, COL9A3, CRYM, DCDC2, DFNA5,
DFNB31, DFNB59, DIABLO, DIAPH1, DIAPH3, DMXL2, DNMT1, DSPP, EDN3,
EDNRB, ELMOD3, EPS8, EPS8L2, ESPN, ESRRB, EYA1, EYA4, FAM189A2,
FAM65B, FGF3, FOXI1, GATA3, GIPC3, GJB1, GJB2, GJB3, GJB4, GJB6, GPSM2,
GRHL2, GRXCR1, GRXCR2, HARS, HARS2, HGF, HOMER2, HSD17B4, ILDR1,
JAG1, KARS, KCNE1, KCNJ10, KCNQ1, KCNQ4, LARS2, LHFPL5, LHX3, LOXHD1,
LRTOMT, MARVELD2, MCM2, MET, MIR96, MITF, MSRB3, MYH14, MYH9, MYO15A,
MYO1A, MYO1C, MYO1F, MYO3A, MYO6, MYO7A, NARS2, NF2, OSBPL2, OTOA,
OTOF, OTOG, OTOGL, P2RX2, PAX3, PCDH15, PDZD7, PEX7, PHYH, PNPT1,
POU3F4, POU4F3, PRPS1, PTPRQ, RDX, S1PR2, SERPINB6, SIX5, SLC17A8,
SLC22A4, SLC26A4, SLC26A5, SLITRK6, SMPX, SNAI2, SOX10, SOX2, SYNE4,
TBC1D24, TECTA, TIMM8A, TJP2, TMC1, TMEM132E, TMIE, TMPRSS3, TMPRSS5,
TNC, TPRN, TRIOBP, TSPEAR, USH1C, USH1G, USH2A, WBP2, WFS1.
Single Gene
EDN3, EDNRB, MITF, PAX3, SNAI2, SOX10, TYR.
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