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70 Possible Causes for Delayed Growth and Development, Night Blindness, Retinal Scar

  • Retinitis Pigmentosa

    According to the researchers, the study suggests controlled electrical stimulation of the retina releases growth factors which may delay degeneration of the retina from RP[allaboutvision.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] The most common form of RP is a rod-cone dystrophy, in which the first symptom is night blindness, followed by the progressive loss in the peripheral visual field in daylight[ncbi.nlm.nih.gov]

  • Retinopathy

    The scarring and bleeding can lead to retinal scarring or detachment from the back of the eye, resulting in vision loss. Why is retinopathy of prematurity a concern?[stanfordchildrens.org] Blood vessels constrict and can become obliterated, resulting in delays of normal retinal vascular development.[emedicine.com] The short duration and rapid progression of symptoms along with the lack of family history of night blindness prompted a diagnosis of autoimmune retinopathy (AIR).[ncbi.nlm.nih.gov]

  • Retinitis

    According to the researchers, the study suggests controlled electrical stimulation of the retina releases growth factors which may delay degeneration of the retina from RP[allaboutvision.com] In young patients with the symptom of night blindness, it is important to differentiate retinitis pigmentosa from stationary night blindness.[ommbid.mhmedical.com] Two patients were not treated (patients 1 and 8), one of whom (patient 8) had received an autologous transplant and was diagnosed with atrophic retinal scarring compatible[academic.oup.com]

  • Fleck Retina of Kandori

    The bleeding causes local irritation and scarring. It can cause retinal detachment. This is a separation of the layers of the retina.[homeopathyworldcommunity.ning.com] Clinical: Growth retardation; delayed development (physical and intellectual); maxillary hypoplasia; micrognathia; large, low-set ears; abnormal motor function; irritability[dentisty.org] * Re:causes of night blindness??[usmleforum.com]

  • Senior-Løken Syndrome

    Prof Yap explained that this condition, associated with retinitis pigmentosa, is characterised by the progressive scarring and development of cysts in both kidneys, leading[nuh.com.sg] This allows prompt symptomatic treatments to be set up which may delay the progression towards end-stage renal failure and prevent the development of complications, such as[jmg.bmj.com] Affected individuals present with slowly progressive restriction of the visual field and night blindness.[neocyst.de]

  • Peripheral Vasoproliferative Retinopathy

    A vasoproliferative tumor of the sensory retina, secondary to presumed congenital toxoplasmosis scars, can cause vitritis and exudative/traction retinal detachment.[link.springer.com] development.[nhp.gov.in] The hallmark symptoms of retinitis pigmentosa are night blindness (nyctalopia) and gradually progressive peripheral visual field loss.[oculist.net]

  • Amaurosis-Hypertrichosis Syndrome

    Detachment, Retinal Haemorrhage, Retinal Tear, Retinal Vein Occlusion, Retinopathy, Retinopathy Hypertensive, Retrograde Amnesia, Rhabdomyolysis, Rheumatoid Arthritis, Rheumatoid[bonkersinstitute.org] […] of growth Digital anomalies with short palpebral slits, atresy oesophagienne or duodénale Anomalies of the channel of muller galactosemy Anomalies of the development of the[wikipedia.qwika.com] Overview Amaurosis hypertrichosis is a rare syndrome characterised by severe retinal dystrophy marked by visual impairment and profound photophobia without night blindness[checkorphan.org]

  • Autosomal Recessive Congenital Cataract 5

    […] can add to this (eg, macular hole formation or retinal detachment ).[patient.info] These techniques may at least delay the need for surgery until a point when eye growth has stabilized and an IOL can be implanted with less refractive uncertainty.[eyewiki.aao.org] A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness. Am J Hum Genet. 2010;87:523–31.[link.springer.com]

  • Malignant Choroidal Melanoma

    Lesion Choroidal nevus Melanocytoma Congenital hypertrophy of retinal pigmented epithelium (CHRPE) Retinal pigmented epithelium hyperplasia Choroidal metastasis Subretinal[webeye.ophth.uiowa.edu] […] or development of orange pigment prior to treatment with plaque radiotherapy. 21 These studies suggest low mortality rates associated with delayed treatment for indeterminate[reviewofophthalmology.com] Fast and slow EOG oscillations in congenital and acquired night blindness. Ophthalmic Res 1979; 11: 206–11. Google Scholar 11. Aschoff U.[link.springer.com]

  • Esotropia

    There are similar rates between the two for serious complications, including periocular infections, retinal tears, and endophthalmitis [12, 14].[webeye.ophth.uiowa.edu] Poor head control Underdeveloped nasal alae Highly arched eyebrow Growth delay Sudden death Abnormality of the nose Flat occiput Punctate cataract Hyperpigmentation of the[mendelian.co] Learn more Other less relevant matches: Low match NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A; CSNB1A Congenital stationary night blindness (CSNB) is a clinically and[mendelian.co]

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