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29 Possible Causes for Focal Atrophy of Choroid, Hemochromatosis

  • Hemochromatosis

    The spectral domain optical coherence tomography showed retinal pigmentary epithelial atrophy associated with irregularities and focal interruption of the ellipsoid zone.[] Hemochromatosis usually occurs in men above the age of 50 years.[] Epub 2015 Jul 8. bronze diabetes bronzed cirrhosis familial hemochromatosis genetic hemochromatosis haemochromatosis HC hemochromatosis hereditary haemochromatosis HH HLAH[]

  • Acute Juvenile Hemorrhagic Cystitis

    […] or choroiditis • Pars plana exudates (“snowbanking”) • Serous, tractional, or rhegmatogenous retinal detachment • Retinochoroidal atrophy • Choroidal and retinal neovascularization[] Annulare Granulomatosis with polyangiitis Griscelli disease type 2 Growth Hormone Deficiency Harlequin syndrome Hashimoto Hashimoto hypothyroidism Hashimoto thyroiditis Hemochromatosis[] Syndrome, AV Malformation, Brain Aneurysm, Cesarean Section, Cystic Hygroma, Disabled Adults, Factor V Leiden, Headaches, Hemangioma and Vascular Malformation, Hereditary Hemochromatosis[]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    Frontometaphyseal dysplasia Gardner syndrome Geroderma osteodysplastica Giant cell glioblastoma Gliosarcoma Glycogen storage disease due to aldolase A deficiency Gyrate atrophy[] Hemochromatosis, Type 2A Hemochromatosis, Type 3 Hemochromatosis, Type 4 Hemolytic Anemia Hemolytic Anemia due to Adenylate Kinase Deficiency Hemolytic Anemia due to Glutathione[] , Type 1 Haemochromatosis Haemochromatosis, Heridtary Hemochromatosis Gene, Included Hemochromatosis, Hereditary Hlah HFE HFE HH 235200 Genetic Test Registry Hereditary Motor[]

  • High Myopia-Sensorineural Deafness Syndrome

    Frontometaphyseal dysplasia Gardner syndrome Geroderma osteodysplastica Giant cell glioblastoma Gliosarcoma Glycogen storage disease due to aldolase A deficiency Gyrate atrophy[] Sialuria, French type Hartnup disease Toriello-Carey syndrome Thompson Baraitser syndrome Periodic fever, aphthous stomatitis, pharyngitis and adenitis Sickle cell anemia Hemochromatosis[] Ehlers-Danlos syndrome with periventricular heterotopia Familial adenomatous polyposis due to 5q22.2 microdeletion Familial idiopathic steroid-resistant nephrotic syndrome with focal[]

  • Familial Hyperaldosteronism Type 1

    […] dystonia - not a rare disease FTSS - See Camptodactyly syndrome Guadalajara type 1 Fuchs atrophia gyrata chorioideae et retinae - See Gyrate atrophy of choroid and retina[] […] of the receptor. rs11953630 EBF1 5q33.3 Early B-cell factor 1, associated with central obesity, B-lymphocytes differentiation and Hodgkin lymphoma. rs1799945 HFE 6p22.2 Hemochromatosis[] See Thyroid cancer, follicular FTD - See Frontotemporal dementia FTH1-related iron overload - See Hemochromatosis type 5 FTLE - See Temporal epilepsy, familial FTSD - See Focal[]

  • Optic Disc Drusen

    Optical coherence tomography (OCT) demonstrated stable focal areas of subretinal fluid OU and macular atrophy OS.[] Other associations include abetalipoproteinemia, acromegaly, diabetes mellitus, facial angiomatosis, hemochromatosis, hemolytic anemia, hereditary spherocytosis, hypercalcinosis[] In addition, a thick choroid with large vessels was noted OU.[]

  • Phakomatosis Pigmentokeratotica

    MRI revealed evidence of focal cortical atrophy, leptomeningeal enhancement, and right choroid plexus enlargement.[] Hemochromatosis and Hemosiderosis ( Joerg Albrecht &Victoria P. Werth ). Primary Biliary Cirrhosis ( Joerg Albrecht & Victoria P.Werth ).[] Hemochromatosis and Hemosiderosis (Joerg Albrecht & Victoria P. Werth). Primary Biliary Cirrhosis (Joerg Albrecht & Victoria P. Werth).[]

  • Mulibrey Nanism Syndrome

    The optic nerve and the macula appeared normal while the midperiphery showed focal choroidal hypoplasia with marked atrophy of the retina and of the pigment epithelium.[] , type 2A; 602390; HJV Hemochromatosis, type 2B; 613313; HAMP Hemochromatosis, type 3; 604250; TFR2 Hemochromatosis, type 4; 606069; SLC40A1 Hemolytic anemia due to adenylate[] By fluorescein angiography areas of focal choroidal hypoplasia were noted.[]

  • Schwartz-Lelek Syndrome

    […] of choroid and retina Hereditary spherocytosis Hypomyelination with atrophy of basal ganglia and cerebellum Hypomyelination with brain stem and spinal cord involvement and[] Gorlin (nevoid basal cell carcinoma) syndrome Greig cephalopolysyndactyly syndrome Hallermann-Streiff syndrome Harlequin fetus Hemophilia A Hereditary hearing loss Hereditary hemochromatosis[] […] myopathy with posterior leg and anterior hand involvement Ehlers-Danlos syndrome with periventricular heterotopia Familial idiopathic steroid-resistant nephrotic syndrome with focal[]

  • Vitreoretinochoroidopathy

    Numerous factors can help differentiate an elevated RPED from a shallow focal retinal detachment: • An RPED obscures the choroidal pattern (this characteristic may abate as[] Hippel-Lindau disease , see von Hippel-Lindau syndrome von Hippel-Lindau syndrome von Passow syndrome , see Horner syndrome Von Recklenhausen-Applebaum disease , see hereditary hemochromatosis[] […] the RPE cells in the RPED atrophy). • The boundary of the RPED typically is better defined than the edge of the retinal detachment. • The light beam reflex is bowed forward[]

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