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Results 1 - 10 of 42 for leber
  1. Leber hereditary optic neuropathy 
    Leber hereditary optic neuropathy (LHON) is an inherited form of vision loss. Although this condition usually begins in a person's teens or twenties, rare cases ...
    https://medlineplus.gov/.../leber-hereditary-optic-neuropathy - Genetics
  2. Leber congenital amaurosis 
    Leber congenital amaurosis, also known as LCA, is an eye disorder that is present from birth (congenital). This condition primarily affects the retina, which ...
    https://medlineplus.gov/.../condition/leber-congenital-amaurosis - Genetics
  3. Leber Congenital Amaurosis (American Association for Pediatric Ophthalmology and Strabismus)  
    Retinal Disorders/Specifics ... Retinal Disorders ... GLOSSARY, TERMS, ACRONYMS, PHRASES, DEFINITIONS, DICTIONARY ... Shows a single glossary entry ... American Association ...
    https://www.aapos.org/glossary/leber-congenital-amaurosis - External Health Links
  4. Senior-Løken syndrome 
    ... called nephronophthisis and an eye condition known as Leber congenital amaurosis.Nephronophthisis causes fluid-filled cysts to ... fluids and waste products from the body effectively.Leber congenital amaurosis primarily affects the retina, which is ...
    https://medlineplus.gov/genetics/condition/senior-loken-syndrome - Genetics
  5. MT-ND1 gene 
    ... the MT-ND1 gene are known to cause Leber hereditary optic neuropathy. Each of these mutations changes ... for about 13 percent of all cases of Leber hereditary optic neuropathy. This mutation replaces the nucleotide ...
    https://medlineplus.gov/genetics/gene/mt-nd1 - Genetics
  6. MT-ND4 gene 
    ... the MT-ND4 gene are known to cause Leber hereditary optic neuropathy. This condition is an inherited ... gene variant is the most common cause of Leber hereditary optic neuropathy; it is responsible for about ...
    https://medlineplus.gov/genetics/gene/mt-nd4 - Genetics
  7. MT-ND6 gene 
    ... ND6 gene have been identified in people with Leber hereditary optic neuropathy. This condition is an inherited ... for about 14 percent of all cases of Leber hereditary optic neuropathy, and it is the most ...
    https://medlineplus.gov/genetics/gene/mt-nd6 - Genetics
  8. CEP290 gene 
    ... the CEP290 gene have been found to cause Leber congenital amaurosis. Leber congenital amaurosis is an eye disorder that primarily ... 15 to 22 percent of all cases of Leber congenital amaurosis. A particular genetic change, written as ...
    https://medlineplus.gov/genetics/gene/cep290 - Genetics
  9. CRB1 gene 
    ... the CRB1 gene have been found to cause Leber congenital amaurosis. Leber congenital amaurosis is an eye disorder that primarily ... Most of the CRB1 gene variants responsible for Leber congenital amaurosis lead to an abnormally short, nonfunctional ...
    https://medlineplus.gov/genetics/gene/crb1 - Genetics
  10. MT-ND4L gene 
    ... gene has been identified in several families with Leber hereditary optic neuropathy. This mutation, which can be ... can lead to the vision loss characteristic of Leber hereditary optic neuropathy. This genetic change appears to ...
    https://medlineplus.gov/genetics/gene/mt-nd4l - Genetics
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