aniridia

[미국]/ˌænəˈraɪdɪə/
[영국]/ˌænəˈraɪdə/

한국어 번역

구문 및 연어

aniridia research

aniridia cases

aniridia patient

aniridia treatment

aniridia diagnosis

aniridia symptoms

aniridia causes

aniridia genetic

aniridia disorder

aniridia management

예문

congenital aniridia is often associated with other ocular abnormalities.

patients with aniridia may develop glaucoma later in life.

genetic testing can confirm mutations in the pax6 gene linked to aniridia.

aniridia can cause severe photophobia due to the lack of iris.

early diagnosis of aniridia is crucial for managing visual development.

surgical options for aniridia include artificial iris implantation.

aniridia management typically involves regular ophthalmologic follow-up.

children with aniridia may require special educational support.

aniridia is a rare condition affecting approximately 1 in 50,000 births.

researchers are investigating new gene therapy approaches for aniridia.

the severity of aniridia varies widely among affected individuals.

support groups provide resources for families dealing with aniridia.

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