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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.[ncbi.nlm.nih.gov] Hemochromatosis usually occurs in men above the age of 50 years.[symptoma.com] Epub 2015 Jul 8. bronze diabetes bronzed cirrhosis familial hemochromatosis genetic hemochromatosis haemochromatosis HC hemochromatosis hereditary haemochromatosis HH HLAH[ghr.nlm.nih.gov]

  • Acute Juvenile Hemorrhagic Cystitis

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

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

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

  • 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[csbg.cnb.csic.es] Sialuria, French type Hartnup disease Toriello-Carey syndrome Thompson Baraitser syndrome Periodic fever, aphthous stomatitis, pharyngitis and adenitis Sickle cell anemia Hemochromatosis[checkrare.com] Ehlers-Danlos syndrome with periventricular heterotopia Familial adenomatous polyposis due to 5q22.2 microdeletion Familial idiopathic steroid-resistant nephrotic syndrome with focal[csbg.cnb.csic.es]

  • 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[rarediseases.info.nih.gov] […] 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[cardiogen.com.ar] See Thyroid cancer, follicular FTD - See Frontotemporal dementia FTH1-related iron overload - See Hemochromatosis type 5 FTLE - See Temporal epilepsy, familial FTSD - See Focal[rarediseases.info.nih.gov]

  • Optic Disc Drusen

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

  • Phakomatosis Pigmentokeratotica

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

  • 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.[eurekamag.com] , type 2A; 602390; HJV Hemochromatosis, type 2B; 613313; HAMP Hemochromatosis, type 3; 604250; TFR2 Hemochromatosis, type 4; 606069; SLC40A1 Hemolytic anemia due to adenylate[howlingpixel.com] By fluorescein angiography areas of focal choroidal hypoplasia were noted.[eurekamag.com]

  • 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[csbg.cnb.csic.es] Gorlin (nevoid basal cell carcinoma) syndrome Greig cephalopolysyndactyly syndrome Hallermann-Streiff syndrome Harlequin fetus Hemophilia A Hereditary hearing loss Hereditary hemochromatosis[berri.es] […] myopathy with posterior leg and anterior hand involvement Ehlers-Danlos syndrome with periventricular heterotopia Familial idiopathic steroid-resistant nephrotic syndrome with focal[csbg.cnb.csic.es]

  • 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[medtextfree.wordpress.com] 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[herenciageneticayenfermedad.blogspot.com] […] 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[medtextfree.wordpress.com]

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