usher syndrome造句
造句与例句手机版
- Mutations within this gene have been associated with Usher syndrome type IIIa.
- People with Usher syndrome represent roughly one-sixth of people with retinitis pigmentosa.
- Jacob Desormeaux, son of horse-racing jockey Kent Desormeaux, has Usher syndrome.
- The progressive blindness of Usher syndrome results from retinitis pigmentosa.
- Usher syndrome is classed into three subtypes according to onset and severity of symptoms.
- Although centered on Great Britain, it offers resources to all people with Usher syndrome.
- A mutation in any one of these genes is likely to result in Usher syndrome.
- Usher syndrome is responsible for the majority of deaf-blindness.
- The simplest approach to diagnosing Usher syndrome is to test for the characteristic chromosomal mutations.
- Christian Markovic is an artist living with Usher syndrome, who runs a company, Fuzzy Wuzzy Designs.
- It's difficult to see usher syndrome in a sentence. 用usher syndrome造句挺难的
- She is a well-known person with Usher syndrome.
- Spencer Tracy's son John Tracy was a well-known person with Usher syndrome who lived a full life.
- A web-community, UsherLife, of people with Usher syndrome, was founded on 1 February 2005 by Nick Sturley.
- Some preliminary studies have suggested as many as 10 % of congenitally deaf children may have Usher syndrome.
- A 31-year-old woman with Usher syndrome, Rebecca Alexander, was profiled in " Marie Claire " in November 2007.
- Those include genes linked to early onset Alzheimer's, spastic paraplegia, NiemannPick disease and a severe form of Usher syndrome.
- Other people with Usher syndrome have posted videos about their lives and condition on YouTube, most notably Ginny Paja-Nyholm.
- Usher syndrome I may be indicated if the child is profoundly deaf from birth and especially slow in walking.
- Syndromic cases occur with diseases such as Usher syndrome, Stickler syndrome, Waardenburg syndrome, Alport's syndrome, and neurofibromatosis type 2.
- Since Usher syndrome is incurable at present, it is helpful to diagnose children well before they develop the characteristic night blindness.
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