The following Conditions are related to Hearing loss

Select a specific condition below to view its details.

  • Autosomal recessive long qt syndrome

    Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is a recessive disorder with congenital deafness and long-QT syndrome. This disorder is a form of long QT syndrome.Symptoms of Autosomal recessive long-QT syndrome may be apparent during early childhood.Sensorineural hearing loss is usually profound, affecting both ears; however, it tends to affect the hearing of high frequencies more than low fr  Read More

  • Jervell and lange-nielsen syndrome

    Jervell and Lange-Nielsen syndrome is a rare genetic illness characterized by congenital deafness that occurs in conjunction with anomalies in the heart's electrical system. The severity of JLNS-related cardiac symptoms varies among individuals. Some people have no symptoms (asymptomatic); others develop abnormally fast heartbeats (tachyarrhythmias), which can cause bouts of unconsciousness, cardiogenic shock, and potential  Read More

  • Sakati-nyhan syndrome

    Sakati-nyhan syndrome is a rare genetic disorder that can cause a variety of complications. It is an autosomal recessive disorder, which means that it happens when you inherit two copies of the gene that causes sakati-nyhan syndrome from both of your parents.The disease is caused by mutations in the HEXA gene on chromosome 19. •The HEXA gene produces a protein called beta-hexosaminidase A (HEXA).  Read More

  • Townes syndrome

    Townes Brocks syndrome is a hereditary disorder that has an impact on several physiological systems. The imperforate anus, dysplastic ears, and hand deformities, which most frequently affect the thumbs, are the characteristics of Townes-Brocks syndrome that are most frequently observed. •These three key characteristics are frequently present in at least two Townes Brocks syndrome patients. •  Read More

  • Velocardiofacial syndrome

    Velocardiofacial syndrome (VCFS) is a genetic disorder that affects the brain and body. It can cause mild to severe medical problems, such as heart defects, hearing loss, cleft lip or palate, developmental delays, and learning disabilities.The disorder is caused by changes in chromosome 22 (one of the 23 pairs of chromosomes found in each cell), which is called a deletion. This means that part of the chromosome has  Read More