Retinal dystrophy

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Classification according to ICD-10
H35.5 Hereditary retinal dystrophy
ICD-10 online (WHO version 2019)

Retinal dystrophy is a group of rare, genetic eye diseases .

According to the Orphanet database , this group contains the following diseases:

Web links

literature

  • EC Davies, R. Pineda: Cataract surgery outcomes and complications in retinal dystrophy patients. In: Canadian journal of ophthalmology. Journal canadien d'ophtalmologie. Volume 52, number 6, December 2017, pp. 543-547, doi: 10.1016 / j.jcjo.2017.04.002 , PMID 29217020 .
  • TC Hohman: Hereditary Retinal Dystrophy. In: Handbook of experimental pharmacology. Volume 242, 2017, pp. 337-367, doi : 10.1007 / 164_2016_91 , PMID 28035529 .

Individual evidence

  1. retinal dystrophy. In: Orphanet (Rare Disease Database).
  2. Åland Iceland eye disease. In: Orphanet (Rare Disease Database).
  3. Amaurosis-Hypertrichosis Syndrome. In: Orphanet (Rare Disease Database).
  4. 3349 Atrophia gyrata of the choroid and retina. In: Orphanet (Rare Disease Database).
  5. Atrophy, bifocal chorioretinal progressive. In: Orphanet (Rare Disease Database).
  6. Autosomal recessive chorioretinopathy-microcephaly syndrome. In: Orphanet (Rare Disease Database).
  7. Bestrophinopathy, autosomal recessive. In: Orphanet (Rare Disease Database).
  8. 17604 Chondrodysplasia, metaphyseal - retinitis pigmentosa. In: Orphanet (Rare Disease Database).
  9. Chorioretinal degeneration, helicoid-peripapillary. In: Orphanet (Rare Disease Database).
  10. Ectopia lentis - chorioretinal dystrophy - myopia. In: Orphanet (Rare Disease Database).
  11. Spotted retina, benign familial. In: Orphanet (Rare Disease Database).
  12. Martinique wrinkled retinal pigment epitheliopathy. In: Orphanet (Rare Disease Database).
  13. Microcorneal myopic chorioretinal atrophy-Telekanthus syndrome. In: Orphanet (Rare Disease Database).
  14. Microcephaly-lymphedema-chorioretinopathy syndrome. In: Orphanet (Rare Disease Database).
  15. MRCS syndrome. In: Orphanet (Rare Disease Database).
  16. Retinal degeneration - nanophthalmos - glaucoma. In: Orphanet (Rare Disease Database).
  17. Retinal dystrophy with dysfunction of the inner retina and ganglion cell abnormalities. In: Orphanet (Rare Disease Database).
  18. Retinal dystrophy, severe, beginning in early childhood. In: Orphanet (Rare Disease Database).
  19. Retinal dystrophy, onset late. In: Orphanet (Rare Disease Database).
  20. Retinal dystrophy type Bothnia. In: Orphanet (Rare Disease Database).
  21. ^ Oguchi disease. In: Orphanet (Rare Disease Database).
  22. Pigmented paravenous retinochoroidal atrophy. In: Orphanet (Rare Disease Database).
  23. Progressive retinal dystrophy due to retinol transport defect. In: Orphanet (Rare Disease Database).
  24. ^ Retinal dysplasia, X-linked. In: Orphanet (Rare Disease Database).
  25. Retinal vasculopathy and cerebral leukoencephalopathy. In: Orphanet (Rare Disease Database).
  26. ^ Revesz syndrome. In: Orphanet (Rare Disease Database).
  27. X-linked intellectual disability-spasticity of the extremities-retinal dystrophy-diabetes insipidus syndrome. In: Orphanet (Rare Disease Database).
  28. Suppository deficiency trichromatism. In: Orphanet (Rare Disease Database).
  29. cone dystrophy with supernormal rod-B-waves. In: Orphanet (Rare Disease Database).
  30. Cerebellar-retinal degeneration, infantile. In: Orphanet (Rare Disease Database).