Create issue ticket

40 Possible Causes for Background Retinopathy, Polydactyly, Progressive Loss of Vision

  • Retinitis Pigmentosa

    Background Retinitis pigmentosa (RP) is a group of eye diseases that affect the retina.[columbiaeye.org] The two siblings showed signs of RP and polydactyly.[ncbi.nlm.nih.gov] A 35-year-old man presented with history of painless, progressive loss of vision in the left eye for the past 7 years.[ncbi.nlm.nih.gov]

  • Retinopathy

    What does it mean if you have 'background retinopathy'?[diabeticretinopathy.org.uk] Neuropathy, motor and sensory, Russe type (Charcot-Marie-Tooth disease type 4G) AD/AR 9 7 IDH3B Retinitis pigmentosa AR 2 3 IFT140 Short -rib thoracic dysplasia with or without polydactyly[blueprintgenetics.com] Over time this causes photoreceptor cells to die and progressive loss of vision results.[retinaaustralia.com.au]

  • Bardet-Biedl Syndrome Type 11

    Diabetic Retinopathy BCK003 Bacteremia 1 BCT019 Bacteremia 2 BCT020 Bacterial Conjunctivitis BCT006 Bacterial Esophagitis BCT001 Bacterial Infectious Disease BCT022 Bacterial[malacards.org] […] recessive form of Bardet-Biedl syndrome (OMIM:209900), a genetically heterogeneous disorder characterised by usually severe pigmentary retinopathy, early-onset obesity, polydactyly[medical-dictionary.thefreedictionary.com] Progressive vision loss due to retinal dystrophy, together with moderate intellectual deficit (when present), behavioral anomalies, hypomimia and obesity will affect the social[orpha.net]

  • Retinitis

    […] eyes than those with background retinopathy in only one or in neither eye.[richtlijnendatabase.nl] The person having BBS also has extra fingers or toes a condition called polydactyly and hypogonadism, a condition affecting the secretion of hormones.[irisvision.com] A loss of side vision, or tunnel vision, is also common as RP progresses.[retinaspecialistsnw.com]

  • Retinitis pigmentosa 40

    Background Retinitis pigmentosa (RP) is a group of eye diseases that affect the retina.[columbiaeye.org] […] disc is pale and there is bilateral widespread black dots or clumps of dots in a pattern like bone spicules on the retina Check for hearing aid and test hearing, don’t miss polydactyly[medicaleducationleeds.com] A loss of side vision, or tunnel vision, also is common as RP progresses.[nweyes.com]

  • Retinal Macular Dystrophy Type 2

    This stage of retinopathy is called non-proliferative or background retinopathy.[avruc.com] Laurence-Moon was described a similar syndrome with spastic paraplegia and no polydactyly.[atlasrleye.com] loss of vision. (10) If both parents carry the ABCA4 mutation, there’s a 25 percent chance that a child will have the condition since it is a recessive gene. (12) No cure[everydayhealth.com]

  • Retinitis Pigmentosa Type 4

    Background Retinitis pigmentosa (RP) is a group of eye diseases that affect the retina.[columbiaeye.org] Laurence-Moon-Biedl syndrome (also called Bardet-Biedl syndrome ): autosomal recessive disorder associated with retinal dystrophy, mental retardation, obesity, hypogonadism, and postaxial polydactyly[unboundmedicine.com] They are characterized by a gradual breakdown and degeneration of photoreceptor cells, which results in a progressive loss of vision.[eyecareinstitute.com]

  • Retinal Pigmentary Dystrophy

    · perivasculitis · varices · vascular sheathing · vasculitis Retinopathy: · NOS · background NOS · Coats · exudative · hypertensive H35.1 Retinopathy of prematurity Retrolental[apps.who.int] Polydactyly is variably present.[uniprot.org] Retinitis pigmentosa (RP) is a group of hereditary retinal diseases, which are characterized by progressive loss of peripheral vision, and...[atlasrleye.com]

  • Obesity

    BACKGROUND: Diabetic retinopathy (DR) was considered to be a common complication of diabetes.[ncbi.nlm.nih.gov] Polydactyly can be associated with ciliopathy. A patient with Bardet-Biedl syndrome requires multi-specialist care.[ncbi.nlm.nih.gov] Cataracts typically progress slowly to cause vision loss and are potentially blinding if untreated.[empoweryourhealth.org]

  • Neuhauser Syndrome

    We describe an Italian family with a peculiar association of microcephaly with retinopathy, short stature, and mild mental retardation in six of its members.[healio.com] Other associated anomalies include brachydactyly, polydactyly as well as renal dysfunction (typically in later life), hepatic dysfunction, and retinal dystrophy.[emedicine.medscape.com] Progressive loss of vision, dyschromatopsia, and photophobia are the primary ocular symptoms. Night blindness and constricted visual fields are noted by some patients.[disorders.eyes.arizona.edu]

Similar symptoms