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797 Possible Causes for Chorioretinopathy, Pediatric Disorder

  • Aicardi's Syndrome

    ., Shevell, M.I. (1998) Infantile epileptic encephalopathy (Ohtahara syndrome) and migrational disorder.[scindeks.ceon.rs] ) are reported together with other unusual cases (isolated lacunar chorioretinopathy).[ncbi.nlm.nih.gov] Nelson Textbook of Pediatrics. 20th ed. Philadelphia, PA: Elsevier; 2016:chap 591. Samat HB, Flores-Samat L. Developmental disorders of the nervous system.[medlineplus.gov]

  • Laurence Moon Syndrome

    […] of the presently known Laurence-Moon syndrome cases, the disease has a childhood onset, characterized by cerebellar ataxia, spastic paraplegia, peripheral neuropathy, and chorioretinopathy[symptoma.com] Pediatr Nephrol. 2012 Jan;27(1):7-15.[de.slideshare.net] Definition An autosomal recessive syndrome characterized by progressive spinocerebellar degeneration, spastic paraplegia, mental retardation, hypogonadism, dwarfism, and chorioretinopathy[uniprot.org]

  • Long Chain Hydroxyacyl-CoA Dehydrogenase Deficiency

    […] subnormal retinal function. ( 27461099 ) Fahnehjelm K.T....NordenstrAPm A. 2016 5 Ultra-Wide-Field Autofluorescence in Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency Chorioretinopathy[malacards.org] Hoffman Pediatric Cardiology (2009) Disorders of mitochondrial long-chain fatty acid oxidation R. J.[dx.doi.org] Chorioretinopathy may also develop over time.[emedicine.medscape.com]

  • Gordon-Holmes Syndrome

    […] inherited disorders and cancer genetics, and on other pediatric adrenal and pituitary disorders.[books.google.de] Chorioretinopathy, Ataxia, and Hypogonadism Clinical Characteristics Ocular Features: The retinal pigment epithelium changes may be seen as early as the first decade of life[disorders.eyes.arizona.edu] Denys-Drash syndrome: relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1. J Pediatr. 1993 Nov. 123(5):673-8. [Medline].[emedicine.medscape.com]

  • Facioscapulohumeral Muscular Dystrophy

    To our knowledge, this patient represents the first reported case of birdshot chorioretinopathy with facioscapulohumeral muscular dystrophy.[joii-journal.springeropen.com] Complications of Neuromuscular Disorders. In Epp, Jr., CH & Bowen Jr., Complications in Pediatric Orthopaedic Surgery, 627-630,1995 Tachdjian M.O.[gait.aidi.udel.edu] Neuromuscul Disord. 2016 Jul;26(7):405-13. doi: 10.1016/j.nmd.2016.04.012. Epub 2016 Apr 22.[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] To propose the notion that vitreal traction may contribute to the pathogenesis of serous detachments in central serous chorioretinopathy (CSC).[readbyqxmd.com] […] inferotemporally for 4-5 clock hours, much less bullous compared to the right eye DIFFERENTIAL DIAGNOSIS Retinal Detachment Hereditary or Acquired Retinoschisis Central Serous Chorioretinopathy[webeye.ophth.uiowa.edu]

  • Varicocele

    Frédérique Vankemmel, Olivia Zambrowski, Pierre Nazeyrollas, Brigitte Delemer, Vincent Durlach, Alain Ducasse and Carl Arndt, Circadian disturbance and idiopathic central serous chorioretinopathy[dx.doi.org] ISBN 978-1682134283. a b "NIMH » Eating Disorders". www.nimh.nih.gov. Retrieved 2019-12-02. a b c d Jameson, Larry (2016). Endocrinology: Adult and Pediatric.[en.wikipedia.org]

  • Richards-Rundle Syndrome

    1 microcephaly and chorioretinopathy 2 microcephaly and chorioretinopathy 3 Microcephaly Deafness Syndrome microcephaly with or without chorioretinopathy, lymphedema, or[rgd.mcw.edu] Corticotrophin-releasing hormone type 1 receptor gene (CRHR1) variants predict posttraumatic stress disorder onset and course in pediatric injury patients.[connects.catalyst.harvard.edu] 1 microcephaly and chorioretinopathy 2 microcephaly and chorioretinopathy 3 Microcephaly Cervical Spine Fusion Anomalies Microcephaly Deafness Syndrome Microcephaly Microphthalmos[rgd.mcw.edu]

  • Hereditary Hyperphosphatasia

    TUBGCP6 Microcephaly with cortical malformations, autosomal recessive type 2 WDR62 Microcephaly with epilepsy and diabetes syndrome IER3IP1 Microcephaly with or without chorioretinopathy[centogene.com] Bone Histomorphometry 383 Chapter 17 A Diagnostic Approach to Skeletal Dysplasias 403 Chapter 26 Familial Hypophosphatemia and Related Disorders 699 Chapter 27 Hereditary[books.google.it] , Autosomal Recessive, 1 1 Microcephaly and Chorioretinopathy, Autosomal Recessive, 2 1 Microcephaly and Chorioretinopathy, Autosomal Recessive, 3 1 Microcephaly with or without[preventiongenetics.com]

  • Congenital Aplastic Anemia

    Po Page 245: dystrophy syndrome Olivopontocerebe Page 249 and 250: defects dysmorphia pelvic dysplasia Page 251 and 252: Chorioretinopathy migration Foetal Page 253 and 254[yumpu.com] Aplastic Anemia Treatment at Dana-Farber/Boston Children's Children and young adults with aplastic anemia are treated at Dana-Farber/Boston Children's Cancer and Blood Disorders[childrenshospital.org] […] national Registry of Neutropenia, the national Registry of Alps and related disorders and the national Data Base of Fanconi Anemia.[elsevier.com]

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