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60 Possible Causes for Late Onset Slowly Progressing Form of Retinitis Pigmentosa, Retinitis Pigmentosa - Late Onset Form

  • Retinitis Pigmentosa 42
  • Retinitis Pigmentosa

    Mono-allelic substitutions in other domains of KLHL7 have been reported in three families affected by a late-onset form of autosomal-dominant retinitis pigmentosa.[ncbi.nlm.nih.gov] One uncommon form of RP called Leber's congenital amaurosis occurs with severe vision loss at birth. Other late-onset forms of RP generally carry a better prognosis.[medicinenet.com] Early onset RP occurs within the first few years of life and is typically associated with syndromic disease forms, while late onset RP emerges from early to mid-adulthood.[en.wikipedia.org]

    Missing: Late Onset Slowly Progressing Form of Retinitis Pigmentosa
  • Cystic Kidney Disease

    form type 1, LRP5 primary osteoporosis AD/AR/Digenic 36 163 MAK Retinitis pigmentosa AR 9 13 MERTK Retinitis pigmentosa AR 18 59 MKKS Bardet-Biedl syndrome, McKusick-Kaufman[blueprintgenetics.com] Faciooculoacousticorenal syndrome AR 15 28 LRP5 * Van Buchem disease, Osteoporosis-pseudoglioma syndrome, Hyperostosis, endosteal, Osteosclerosis, Exudative vitreoretinopathy, Osteopetrosis late-onset[blueprintgenetics.com]

    Missing: Late Onset Slowly Progressing Form of Retinitis Pigmentosa
  • Infantile Choroidocerebral Calcification Syndrome

    Late onset Batten disease. Neuronal ceroid lipofuscinosis late infantile form. Jansky-Bielschowsky Disease. Early onset Batten disease.[neurometplus.com] Neuropathy, ataxia and retinitis pigmentosa (NARP) Nezelof Syndrome. Combined Immunodeficiency. Niemann-Pick Disease type A (early infantile).[neurometplus.com]

    Missing: Late Onset Slowly Progressing Form of Retinitis Pigmentosa
  • Pelizaeus-Merzbacher Disease

    There is also a second, congenital, recessively inherited form marked by late onset with a faster course, and a dominant form with onset in adulthood, marked by photosensitivity[whonamedit.com] […] of the skin, dwarfism, cerebellar ataxia, corticospinal signs, cataracts, retinitis pigmentosa, and deafness.[whonamedit.com]

    Missing: Late Onset Slowly Progressing Form of Retinitis Pigmentosa
  • Autosomal Dominant Spastic Paraplegia Type 6

    Most cases of SPG10 represent a pure form of HSP with late onset.[flybase.org] Complex forms may occur with additional symptoms including upper limb amyotrophy, intellectual disability, hearing loss and retinitis pigmentosa.[flybase.org]

    Missing: Late Onset Slowly Progressing Form of Retinitis Pigmentosa
  • Autosomal Dominant Spastic Paraplegia Type 17

    Most cases of SPG10 represent a pure form of HSP with late onset.[flybase.org] Complex forms may occur with additional symptoms including upper limb amyotrophy, intellectual disability, hearing loss and retinitis pigmentosa.[flybase.org]

    Missing: Late Onset Slowly Progressing Form of Retinitis Pigmentosa
  • Autosomal Dominant Spastic Paraplegia Type 31

    Most cases of SPG10 represent a pure form of HSP with late onset.[flybase.org] Complex forms may occur with additional symptoms including upper limb amyotrophy, intellectual disability, hearing loss and retinitis pigmentosa.[flybase.org]

    Missing: Late Onset Slowly Progressing Form of Retinitis Pigmentosa
  • Autosomal Dominant Spastic Paraplegia Type 29

    Most cases of SPG10 represent a pure form of HSP with late onset.[flybase.org] Complex forms may occur with additional symptoms including upper limb amyotrophy, intellectual disability, hearing loss and retinitis pigmentosa.[flybase.org]

    Missing: Late Onset Slowly Progressing Form of Retinitis Pigmentosa
  • Autosomal Dominant Spastic Paraplegia Type 10

    Most cases of SPG10 represent a pure form of HSP with late onset.[flybase.org] Complex forms may occur with additional symptoms including upper limb amyotrophy, intellectual disability, hearing loss and retinitis pigmentosa.[flybase.org]

    Missing: Late Onset Slowly Progressing Form of Retinitis Pigmentosa

Further symptoms