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Usher "Syndrome," Type III
- Usher syndrome is a condition characterized by partial or total hearing loss and vision loss that worsens over time. The hearing loss is classified as sensorineural, ...
- ... CLRN1 gene have been identified in people with Usher syndrome type III, which is characterized by a combination ... cause a form of the condition known as Usher syndrome type IIIA (USH3A). This form of Usher syndrome ...
- ... suggested that individuals with DFNB2 may actually have Usher syndrome (described below), because some individuals who were thought ... developed retinitis pigmentosa (a vision disorder characteristic of Usher syndrome) later in life. However, other individuals diagnosed with ...
- ... as part of a genetic syndrome (such as Usher syndrome, described below).The USH2A gene mutations that cause ... USH2A gene have been identified in people with Usher syndrome type II, which is characterized by a combination ...
- ... caused by a CDH23 mutation may actually have Usher syndrome (described below). A few children thought to have ... pigmentosa later in life, which is characteristic of Usher syndrome. More About This Health Condition More than 60 ...
- ... anemia Sjögren-Larsson syndrome Tay-Sachs disease Tyrosinemia Usher syndrome Zellweger spectrum disorder , also called Zellweger syndrome spectrum ...
- ... most common form of syndromic retinitis pigmentosa is Usher syndrome, which is characterized by the combination of vision ...
- ... cause syndromic forms of hearing loss, such as Usher syndrome (CDH23 and MYO7A, among others), Pendred syndrome (SLC26A4), ...
