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96 Possible Causes for Central Diabetes Insipidus, Chorioretinitis, Progressive Loss of Vision

  • Syphilis

    For emergency physicians it is important to be aware of iritis, uveitis, or chorioretinitis as ocular manifestations of neurosyphilis especially in this high-risk population[] Abstract We present a case of ocular syphilis after a renal transplantation involving progressive vision loss without clinically identifiable ocular disease.[] […] secondary syphilis convert 091.4 to ICD-10-CM 091.5 Uveitis due to secondary syphilis 091.50 Syphilitic uveitis, unspecified convert 091.50 to ICD-10-CM 091.51 Syphilitic chorioretinitis[]

  • Congenital Toxoplasmosis

    Congenital toxoplasmosis can contribute to the development of central diabetes insipidus in infants.[] In congenital cases, ocular toxoplasmosis often presents as a focal whitish fluffy lesion in the retina adjacent to an inactive chorioretinal scar.[] If the central structures of the retina are involved there will be a progressive loss of vision that can lead to blindness.[]

  • Toxoplasmosis

    Nitta A, Suzumura H, Kano K, Arisaka O (2006) Congenital toxoplasmosis complicated with central diabetes insipidus in the first week of life.[] We report the first SS-OCT images of an acute case of toxoplasmosis chorioretinitis.[] If the central structures of the retina are involved there will be a progressive loss of vision that can lead to blindness.[]

  • Suprasellar Tumor

    Germinoma responsible for central diabetes insipidus.[] We are aware of but one other reported case. 2 In the latter, see-saw nystagmus was noted in a patient with extremely low vision attributed to toxoplasma chorioretinitis.[] loss of vision for four years.[]

  • Optic Atrophy

    Wolfram syndrome (WS) is an autosomal recessive neurodegenerative disorder characterized by diabetes mellitus (DM), optic atrophy (OA), central diabetes insipidus (CDI) and[] […] albipunctatus Fundus pulverulentus GAPO syndrome Genetic macular dystrophy Goldmann-Favre syndrome Gyrate atrophy of choroid and retina HERNS syndrome Helicoid peripapillary chorioretinal[] A 36-year-old man presented to the emergency department because of gradual blurring of vision in his right eye over 20 days and progressive loss of vision in the left eye[]

  • Wagner Disease

    JAN 2002; 46 (1) : 279-280 Shin-JH; Lee-HK; Choi-CG; Suh-DC; Kim-CJ; Hong-SK; Na-DG MR Imaging of central diabetes insipidus: A pictorial essay KOREAN-JOURNAL-OF-RADIOLOGY[] Wagner syndrome (WGN1; MIM 143200), an autosomal dominant vitreoretinopathy characterized by chorioretinal atrophy, cataract, and retinal detachment, is linked to 5q14.3.[] Wagner syndrome is a hereditary disorder that causes progressive vision loss.[]

  • Disseminated Toxoplasmosis

    Congenital toxoplasmosis complicated by central diabetes insipidus in an infant with Down syndrome. Brain Dev. 1996; 18 (1): 75-7[ PubMed ] 11. Cavallazzi LO.[] See also separate Chorioretinal Inflammation article.[] If the central structures of the retina are involved there will be a progressive loss of vision that can lead to blindness.[]

  • Neuronal Ceroid Lipofuscinosis

    diabetes insipidus Hereditary cerebral cavernoma Hereditary cerebral cavernous malformation Hereditary cerebral hemorrhage with amyloidosis, Arctic type Hereditary cerebral[] Most childhood forms of NCL are clinically characterized by progressive loss of vision as well as mental and motor deterioration, epileptic seizures, and premature death,[] The juvenile form of neuronal ceroid lipofuscinosis (JNCL) is caused by mutations in the CLN3 gene, and is characterized by progressive loss of vision and development of motor[]

  • Erdheim-Chester Disease

    At our rheumatologic department we compiled his recent medical history, which consisted of diagnosis of central diabetes insipidus, hyperprolactinemia and secondary hypogonadism[] Chorioretinal biopsy confirmed the diagnosis of ECD in 1 case, with the presence of histiocytic infiltration, fibrosis, and characteristic immunohistologic staining.[] During hospitalization, the progression was unfavorable; proptosis progressed, causing a severe loss of vision in the left eye (from 0.8 Snellen to NLP).[]

  • Sorsby Syndrome

    Abstract A familial condition characterized by juvenile diabetes mellitus (DM), optic atrophy (OA), nerve deafness (D), diabetes insipidus (DI) and central nervous system[] Type your tag names separated by a space and hit enter Links Authors , , Source MeSH Chorioretinitis Female Humans Middle Aged Pseudoxanthoma Elasticum Pub Type(s) Case Reports[] Retinitis pigmentosa (RP) is a group of hereditary retinal diseases, which are characterized by progressive loss of peripheral vision, and...[]

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