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Results 1 - 10 of 49 for Retinitis pigmentosa 4
  1. Retinitis pigmentosa 
    ... Central Fahim AT, Daiger SP, Weleber RG. Nonsyndromic Retinitis Pigmentosa Overview. 2000 Aug 4 [updated 2023 Apr 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews(R) ... Hamel C. Retinitis pigmentosa. Orphanet J Rare Dis. 2006 Oct 11;1: ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  2. RPGR gene 
    ... within a new RPGR exon in X-linked retinitis pigmentosa. Nat Genet. 2000 Aug;25(4):462-6. doi: 10.1038/78182. Citation on ...
    https://medlineplus.gov/genetics/gene/rpgr - Genetics
  3. RP2 gene 
    ... Positional cloning of the gene for X-linked retinitis pigmentosa 2. Nat Genet. 1998 Aug;19(4):327-32. doi: 10.1038/1214. Citation on ...
    https://medlineplus.gov/genetics/gene/rp2 - Genetics
  4. RHO gene 
    ... Cheetham ME. Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy. Trends Mol Med. 2005 Apr;11(4):177-85. doi: 10.1016/j.molmed.2005. ...
    https://medlineplus.gov/genetics/gene/rho - Genetics
  5. Usher Syndrome From the National Institutes of Health (National Institute on Deafness and Other Communication Disorders)  
    Usher Syndrome/Learn More ... Usher Syndrome ... Usher syndrome is the most common condition that affects both hearing and vision; sometimes it also affects balance. ...
    https://www.nidcd.nih.gov/health/usher-syndrome - External Health Links
  6. Retinitis pigmentosa 
    ... main risk factor is a family history of retinitis pigmentosa. It is a rare condition affecting about 1 in 4,000 people in the United States.
    https://medlineplus.gov/ency/article/001029.htm - Medical Encyclopedia
  7. ABCA4 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Retinitis pigmentosa More About This Health Condition ABCA4_HUMAN ABCR ATP-binding cassette sub-family A member 4 ATP-binding cassette transporter, retinal-specific ATP-binding ...
    https://medlineplus.gov/genetics/gene/abca4 - Genetics
  8. Usher syndrome 
    ... have profound hearing loss. Vision loss caused by retinitis pigmentosa also develops in late childhood or adolescence. Some people with Usher syndrome type III develop vestibular abnormalities that cause problems with balance. Usher syndrome affects around 4 to 17 in 100,000 people. Types I ...
    https://medlineplus.gov/genetics/condition/usher-syndrome - Genetics
  9. Cold-induced sweating syndrome 
    ... Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa. Am J Hum Genet. 2016 Jul 7;99(1):236-45. doi: 10.1016/j.ajhg.2016.05.026. Erratum In: Am J Hum Genet. 2018 Apr 5;102(4):713. doi: 10.1016/j.ajhg.2018.03. ...
    https://medlineplus.gov/.../condition/cold-induced-sweating-syndrome - Genetics
  10. Vitelliform macular dystrophy 
    ... retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or ... other maculopathies. Hum Mutat. 2000;15(4):301-8. doi: 10.1002/(SICI)1098-1004( ...
    https://medlineplus.gov/.../condition/vitelliform-macular-dystrophy - Genetics
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