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135 Possible Causes for Laurence Moon Syndrome, Night Blindness, Retinal Vessels Attenuated

  • Retinitis pigmentosa 40

    vessel attenuation and waxy pallor of the optic nerve Posterior subcapsular cataracts characterized by yellowish crystalline changes in the visual axis of the posterior lens[centogene.com] 6, congenital, X-linked GPR179 Congenital stationary night blindness, type 1E GRIP1 Cryptophthalmos syndrome GRK1 Oguchi disease 2 GRM6 Congenital stationary night blindness[asperbio.com] Syndromic RP: Usher’s Syndrome; congenital deafness and RP, balance problems Laurence-Moon Syndrome or Bardet-Biedl Syndrome; obese, deaf, hypogonadism, dwarfism, renal failure[medicaleducationleeds.com]

  • Retinitis Pigmentosa

    vessel attenuation and waxy pallor of the optic nerve Posterior subcapsular cataracts characterized by yellowish crystalline changes in the visual axis of the posterior lens[centogene.com] The left eye of the same patient revealed typical PPRCA phenotype, with no night blindness, normal field, and normal ERG.[ncbi.nlm.nih.gov] Short stature, renal dysfunction, and polydactyly are some signs of Bardet-Biedl syndrome or Laurence-Moon syndrome when associated with pigmentary retinopathy.[patient.info]

  • Retinitis

    vessel attenuation and waxy pallor of the optic nerve Posterior subcapsular cataracts characterized by yellowish crystalline changes in the visual axis of the posterior lens[centogene.com] In young patients with the symptom of night blindness, it is important to differentiate retinitis pigmentosa from stationary night blindness.[ommbid.mhmedical.com] Short stature, renal dysfunction, and polydactyly are some signs of Bardet-Biedl syndrome or Laurence-Moon syndrome when associated with pigmentary retinopathy.[patient.info]

  • Laurence Moon Syndrome

    His fundus showed pale, waxy discs with marked attenuation of vessels and typical picture of retinitis pigmentosa [Figure - 2] with some degenerative changes in the maculae[ijo.in] syndrome LAURENCE-MOON SYNDROME LNMS LAURENCE-MOON SYNDROME; LNMS edit English Laurence-Moon syndrome rare autosomal recessive genetic disorder associated with retinitis[wikidata.org] Laurence Moon syndrome is a rare genetic disease of a multisystemic nature that features hypopituitarism, obesity, mental retardation, ataxia, and retinal dystrophy.[symptoma.com]

  • Boucher-Neuhauser Syndrome

    Retinal vessels may be attenuated. Progressive loss of vision, dyschromatopsia, and photophobia are the primary ocular symptoms.[disorders.eyes.arizona.edu] Synonyms of Laurence-Moon Syndrome adipogenital-retinitis pigmentosa syndrome LNMS LMS General Discussion Summary Laurence-Moon syndrome (LNMS) is a genetic condition that[rarediseases.org] The clinical features of Refsum's disease include cerebellar ataxia and retinal dystrophy with pigment changes, bone-spicule formation, optic atrophy, and attenuated retinal[synapse.koreamed.org]

  • Retinitis Pigmentosa 30

    vessel attenuation and waxy pallor of the optic nerve Posterior subcapsular cataracts characterized by yellowish crystalline changes in the visual axis of the posterior lens[centogene.com] In young patients with the symptom of night blindness, it is important to differentiate retinitis pigmentosa from stationary night blindness.[ommbid.mhmedical.com] Many other conditions have similarities to retinitis pigmentosa, including: Friedreich's ataxia Laurence-Moon syndrome (also called Laurence-Moon-Bardet-Biedl syndrome) Mucopolysaccharidosis[iloveicare.co.nz]

  • Retinitis Pigmentosa 7

    The macula looks smooth and normal; however, the retinal vessels are attenuated and there are bone spicules throughout the periphery. OS: Vertical C/D ratio is 0.0.[retinagallery.com] In young patients with the symptom of night blindness, it is important to differentiate retinitis pigmentosa from stationary night blindness.[ommbid.mhmedical.com] Short stature, renal dysfunction, and polydactyly are some signs of Bardet-Biedl syndrome or Laurence-Moon syndrome when associated with pigmentary retinopathy.[patient.info]

  • Sorsby Syndrome

    Attenuation of the retinal vessels evolves with disease progression.[atlasrleye.com] blindness, congenital stationary CACNA1F Aland Island eye disease, Cone rod dystrophy, Night blindness, congenital stationary CACNA2D4 Retinal cone dystrophy CC2D2A COACH[molecularvisionlab.com] Abstract The Laurence-Moon-Biedl syndrome was first described by Laurence and M o on in the British Journal of Ophthalmology in 1866.[mdedge.com]

  • Bardet-Biedl Syndrome Type 11

    Optic disks and retinal vessels are normal in infancy; disk pallor and attenuated retinal vessels develop with age.[scielo.br] Case Report A 12-year-old boy presented to the pediatric outpatient department with the complaint of night blindness.[mjdrdypu.org] How Is Laurence-Moon Syndrome Diagnosed?[familyconnect.org]

  • Retinitis Pigmentosa Type 4

    vessel attenuation and waxy pallor of the optic nerve Posterior subcapsular cataracts characterized by yellowish crystalline changes in the visual axis of the posterior lens[centogene.com] In young patients with the symptom of night blindness, it is important to differentiate retinitis pigmentosa from stationary night blindness.[ommbid.mhmedical.com] Short stature, renal dysfunction, and polydactyly are some signs of Bardet-Biedl syndrome or Laurence-Moon syndrome when associated with pigmentary retinopathy.[patient.info]

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