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ENT/Hearing Loss

ENT Disorders

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.

Genetics of ENT Disorders

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.

Who needs to get tested?

Here’s some common disorders where genetic testing might of help in diagnosis:


  • Hearing Loss: Mutations in genes responsible for the development and function of the inner ear can lead to hearing impairment. For example, mutations in the GJB2 gene are a common cause of hereditary hearing loss.
  • Chronic Sinusitis: remains a complex condition influenced by multiple factors, including genetics. Research indicates that certain genes can affect immune system function, making individuals more susceptible to chronic sinus infections. Those with genetic conditions such as cystic fibrosis often experience chronic sinusitis due to thickened mucus secretions
  • Sleep Apnea: characterized by interrupted breathing during sleep, can have genetic ties. Family history is a known risk factor, and studies have identified genetic markers associated with the condition. These genetic factors can influence the structure of the airway or the regulation of breathing patterns during sleep.
  • Ear Disorders: Ear infections, especially in children, are a common ENT problem. While environmental factors like exposure to smoke or germs can trigger infections, genetics can make some individuals more susceptible. For instance, researchers have found that certain genetic mutations can affect parts of the inner ear, increasing the risk of infections or even hearing loss.
  • Nose and Sinus Disorders: Ever wonder why you seem to have a runny nose all the time, while others walk around sniffle-free? Your nasal and sinus health can also be influenced by your genes. Chronic sinusitis—an inflammation of the sinuses that lasts for a long time—can often be linked to genetic factors. If someone in your family has had a history of sinus issues, there’s a possibility you might inherit this trait.
  • Throat Disorders: When it comes to the throat, tonsillitis is a common disorder with potential genetic ties. Tonsillitis occurs when the tonsils become inflamed, usually due to infection. While anyone can get tonsillitis, repeated episodes can indicate a genetic predisposition. Furthermore, some studies suggest that genetic factors can affect how our immune system responds to these infections.
  • Allergies and Genetic Predispositions: Allergies are another area where genetics play a starring role. If you’re allergic to something, there’s a good chance someone else in your family is too. Allergies occur when the immune system overreacts to certain substances, and while they can develop at any age, they are often seen in families. Common allergens include pollen, dust, food and pet dander. If one of your parents has allergies, you have about a 30% chance of developing them too. If both parents have allergies, your chances climb to around 60-70%. Though the environment and lifestyle can influence how these allergies manifest, your genetic makeup sets the stage.

How are results valuable to you and your family’s health?

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.

Panels and Tests

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.


📍Jabal Amman-5th Circle-Opposite of Arab Medical Center Hospital

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