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541 Possible Causes for Chorioretinopathy, Congenital Eye Anomaly

  • Choroid Hemangioma

    Arash Maleki,Arezoo Astaraki,Ahad Sedaghat,Ramin Jaberi,Stacey Lee,Zohreh Azma,Sukhum Silpa-Archa Retina. 2018; 38(5): 1024 7 Elevated Choroidal Thickness and Central Serous Chorioretinopathy[jovr.org] anomaly whereby the eye is shorter than normal, develops a cataract, and may present with whitening of the pupil.[murraymd.com] These include central serous chorioretinopathy, choroidal melanoma, choroidal metastasis, posterior nodular scleritis, and non-specific retinal detachment.[journalofoptometry.org]

  • Ectopia Lentis

    We report a case of ectopia lentis and central serous chorioretinopathy in a young female patient with several manifestations of Marfan syndrome in the skeletal, cardiovascular[ncbi.nlm.nih.gov] Category Congenital malformation Brite Human diseases [BR: br08402 ] Congenital malformations Congenital malformations of eye H00662 Ectopia lentis Human diseases in ICD-11[genome.jp] Abstract Keratolenticular dysgenesis (KLD) and ectopia lentis are congenital eye defects.[ncbi.nlm.nih.gov]

  • Foveal Retinoschisis

    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 57 ( 12 ) 2016年09月 [査読有り] Fundus Autofluorescence at Test Irradiation Spots after Selective Retina Therapy for Central Serous Chorioretinopathy[research-soran17.osaka-cu.ac.jp] Eyes having optic disc anomalies including congenital optic disc pit or coloboma, intrachoroidal cavitation, [10] a history of ocular surgery other than cataract extraction[journals.plos.org] To propose the notion that vitreal traction may contribute to the pathogenesis of serous detachments in central serous chorioretinopathy (CSC).[readbyqxmd.com]

  • Congenital Optic Disc Coloboma

    Among them, serous retinal detachment that may mimic central serous chorioretinopathy is known to be a common complication.[entokey.com] Isolated and total optic disc coloboma is a markedly rare congenital anomaly of the eye.[ncbi.nlm.nih.gov] Enhanced depth imaging optical coherence tomography of the choroid in central serous chorioretinopathy. Retina. 2009;29:1469–1473. 23.[e-tjo.org]

  • Hallermann-Streiff Syndrome

    1 microcephaly and chorioretinopathy 2 microcephaly and chorioretinopathy 3 Microcephaly Deafness Syndrome microcephaly with or without chorioretinopathy, lymphedema, or[rgd.mcw.edu] Hallermann-Streiff syndrome is a rare congenital disorder characterized as a complex association of developmental anomalies involving structures of ectodermal origin (the[ncbi.nlm.nih.gov] Brachycephaly is also a typical feature, but this cannot be determined from the painting. (2) Congenital anomalies of the eyes seen in La Niña include microphthalmia, microcornea[healio.com]

  • Congenital Rubella Syndrome

    Although uncommon, central serous chorioretinopathy can occur in anatomically small eyes after trabeculectomy surgery.[ncbi.nlm.nih.gov] .  Rate of organ anomalies in CRS 5.  The classic triad for congenital rubella syndrome is:  Sensorineural deafness (58% of patients)  Eye abnormalities especially pigmentary[slideshare.net] To describe a case of central serous chorioretinopathy after trabeculectomy surgery in an eye with microphthalmos in the setting of congenital rubella syndrome.[ncbi.nlm.nih.gov]

  • Stickler Syndrome

    […] syndrome Chromosome 1q41-q42 deletion syndrome Acrocapitofemoral dysplasia Hereditary geniospasm Craniometaphyseal dysplasia, autosomal dominant Lymphedema, microcephaly and chorioretinopathy[checkrare.com] The vitreous showed distinct abnormalities consistent with congenital vitreous anomaly of type 1 Stickler syndrome.[ncbi.nlm.nih.gov] Glaucoma Vitreal anomalies (gel that fills the eye).[en.wikibooks.org]

  • Melhem-Fahl Syndrome

    1 microcephaly and chorioretinopathy 2 microcephaly and chorioretinopathy 3 Microcephaly Deafness Syndrome Microcephaly Seizures Mental Retardation Heart Disorders microcephaly[rgd.mcw.edu] […] dystrophy congenital infantile cataract hypogonadism Muscular dystrophy congenital, merosin negative Muscular dystrophy facioscapulohumeral Muscular dystrophy limb girdle[mindmappedia.com] Microcephaly seizures mental retardation heart disorders Microcephaly sparse hair mental retardation seizures Microcephaly syndactyly brachymesophalangy Microcephaly with chorioretinopathy[statemaster.com]

  • Mononen-Karnes-Senac Syndrome

    […] anomalies syndrome 3 Cases 457351 Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome 14 Cases 2526 Microcephaly-lymphedema- chorioretinopathy[azkurs.org] […] with brain and eye anomalies A3 - See Muscle eye brain disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, DAG1-RELATED - See Limb-girdle muscular dystrophy type[herenciageneticayenfermedad.blogspot.com] Microcephaly seizures mental retardation heart disorders Microcephaly sparse hair mental retardation seizures Microcephaly syndactyly brachymesophalangy Microcephaly with chorioretinopathy[mindmappedia.com]

  • Retinal Pigmentary Dystrophy

    Retinoschisis, x-chromosomal Vitamin-A-Mangel X-chromosomale Retinoschisis Autoimmunerkrankungen mit Netzhaut- Aderhautdegeneration Carcinom assoziierte Retinopathie Birdshot-Chorioretinopathie[drdiag.hu] […] pigment epithelium H35.6 Retinal hemorrhage H35.60 …… unspecified eye H35.7 Separation of retinal layers H35.70 Unspecified separation of retinal layers H35.71 Central serous chorioretinopathy[icd10data.com] […] pigmentary)(vitelliform) · tapetoretinal · vitreoretinal Retinitis pigmentosa Stargardt's disease H35.6 Retinal haemorrhage H35.7 Separation of retinal layers Central serous chorioretinopathy[apps.who.int]

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