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Results 1 - 9 of 9 for Retinitis pigmentosa 42
  1. PRPH2 gene 
    ... Saperstein DA, Sullivan LS. Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies. Hum Mutat. 2001;17(1):42-51. doi: 10.1002/1098-1004(2001)17: ...
    https://medlineplus.gov/genetics/gene/prph2 - Genetics
  2. Usher syndrome 
    ... El-Amraoui A. Usher syndrome (sensorineural deafness and retinitis pigmentosa): pathogenesis, molecular diagnosis and therapeutic approaches. Curr Opin Neurol. 2012 Feb;25(1):42-9. doi: 10.1097/WCO.0b013e32834ef8b2. Citation on ...
    https://medlineplus.gov/genetics/condition/usher-syndrome - Genetics
  3. TTPA gene 
    ... T, Harino S, Suzuki J. Clinicopathological report of retinitis pigmentosa with vitamin E ... doi: 10.1021/bi060522c. Citation on PubMed Yokota ...
    https://medlineplus.gov/genetics/gene/ttpa - Genetics
  4. Ataxia with vitamin E deficiency 
    ... T, Harino S, Suzuki J. Clinicopathological report of retinitis pigmentosa with vitamin E deficiency ... Citation on PubMed
    https://medlineplus.gov/.../ataxia-with-vitamin-e-deficiency - Genetics
  5. Abetalipoproteinemia 
    ... condition may also develop an eye disorder called retinitis pigmentosa, in which breakdown of the light-sensitive layer ( ... cause vision loss. In individuals with abetalipoproteinemia, the retinitis pigmentosa can result in complete vision loss. People with ...
    https://medlineplus.gov/genetics/condition/abetalipoproteinemia - Genetics
  6. Senior-Løken syndrome 
    ... Hildebrandt F. A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution. ...
    https://medlineplus.gov/genetics/condition/senior-loken-syndrome - Genetics
  7. Nearsightedness 
    ... congenital stationary night blindness, Stickler syndrome, Marfan syndrome, retinitis pigmentosa, cone-rod dystrophy, deafness and myopia syndrome, Knobloch ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics
  8. Cone-rod dystrophy 
    ... of rod-cone dystrophy is a condition called retinitis pigmentosa. ABCA4 CACNA1F CNGA3 CNGB3 CRB1 CRX GUCY2D PDE6C ...
    https://medlineplus.gov/genetics/condition/cone-rod-dystrophy - Genetics
  9. PDE6B gene 
    ... This Health Condition MedlinePlus Genetics provides information about Retinitis pigmentosa More About This Health Condition GMP-PDE beta ...
    https://medlineplus.gov/genetics/gene/pde6b - Genetics