Retinal dystrophy
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:
- Acaeruloplasminemia
- Åland Island Eye Disease , synonyms: albinism, ocular, Forsius-Eriksson type; Forsius-Eriksson Syndrome
- Amaurosis-Hypertrichosis Syndrome , Synonym: Jalili Syndrome
- Leber Congenital Amaurosis
- Atrophia gyrata of the choroid and retina , synonyms: HOGA; Hyperornithinemia ; Hyperornithinemia - atrophia gyrata of the choroid and retina; Ornithine aminotransferase deficiency
- Progressive bifocal chorioretinal atrophy , synonym: PBCRA
- Autosomal recessive chorioretinopathy-microcephaly syndrome , synonym: pseudotoxoplasmosis syndrome (The synonym is also used for Aicardi-Goutières syndrome .)
- Burgess-Black retinopathy
- Chondrodysplasia, metaphyseal - retinitis pigmentosa
- Helicoid-peripapillary chorioretinal degeneration, synonyms: Atrophia areata; Degeneration, chorioretinal, Sveinsson type
- Noble Bass Sherman Syndrome
- Benign familial spotted retina
- Martinique wrinkled retinal pigment epitheliopathy
- MMCAT syndrome
- Microcephaly-lymphedema-chorioretinopathy syndrome, synonym: MLCRD
- MORM syndrome
- MRCS syndrome , synonym: microcornea - cone-rod dystrophy - cataract - posterior staphyloma
- Retinal Degeneration - Nanophthalmos - Glaucoma
- Retinal dystrophy with dysfunction of the inner retina and ganglion cell abnormalities
- Early onset severe retinal dystrophy , synonym: EOSRD
- Late onset retinal dystrophy , synonyms: LORD; Retinal dystrophy, autosomal dominant, late onset
- Retinal dystrophy type Bothnia , synonym: Västerbotten dystrophy
- Oguchi Syndrome , Synonyms: Oguchi Disease; Inpatient night blindness, congenital, Oguchi type
- Pigmented paravenous retinochoroid atrophy , synonym PPRCA
- Progressive retinal dystrophy due to retinol transport defect , synonym: retinal dystrophy-iris coloboma-comedogenic acne syndrome
- X-linked retinal dysplasia
- Retinal vasculopathy and cerebral leukoencephalopathy , synonym: RVCL
- Retinopathia pigmentosa
- Revesz syndrome , synonyms: Dyskeratosis congenita with bilateral exudative retinopathy; Retinopathy - anemia - CNS abnormalities; Revesz-Debuse Syndrome
- X-linked intellectual disability-extremity spasticity-retinal dystrophy-diabetes insipidus syndrome
- Suppository deficiency trichromasia , synonym: suppository deficiency syndrome
- Cone dystrophy with super normal rod B waves , synonyms: cone dystrophy with super normal whole field electroretinogram; Cone dystrophy with super normal rod ERG; Cone dystrophy with a super normal rod electroretinogram
- Mitochondrial aconitas deficiency , synonym: cerebellar-retinal degeneration, infantile
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
- ↑ retinal dystrophy. In: Orphanet (Rare Disease Database).
- ↑ Åland Iceland eye disease. In: Orphanet (Rare Disease Database).
- ↑ Amaurosis-Hypertrichosis Syndrome. In: Orphanet (Rare Disease Database).
- ↑ 3349 Atrophia gyrata of the choroid and retina. In: Orphanet (Rare Disease Database).
- ↑ Atrophy, bifocal chorioretinal progressive. In: Orphanet (Rare Disease Database).
- ↑ Autosomal recessive chorioretinopathy-microcephaly syndrome. In: Orphanet (Rare Disease Database).
- ↑ Bestrophinopathy, autosomal recessive. In: Orphanet (Rare Disease Database).
- ↑ 17604 Chondrodysplasia, metaphyseal - retinitis pigmentosa. In: Orphanet (Rare Disease Database).
- ↑ Chorioretinal degeneration, helicoid-peripapillary. In: Orphanet (Rare Disease Database).
- ↑ Ectopia lentis - chorioretinal dystrophy - myopia. In: Orphanet (Rare Disease Database).
- ↑ Spotted retina, benign familial. In: Orphanet (Rare Disease Database).
- ↑ Martinique wrinkled retinal pigment epitheliopathy. In: Orphanet (Rare Disease Database).
- ↑ Microcorneal myopic chorioretinal atrophy-Telekanthus syndrome. In: Orphanet (Rare Disease Database).
- ↑ Microcephaly-lymphedema-chorioretinopathy syndrome. In: Orphanet (Rare Disease Database).
- ↑ MRCS syndrome. In: Orphanet (Rare Disease Database).
- ↑ Retinal degeneration - nanophthalmos - glaucoma. In: Orphanet (Rare Disease Database).
- ↑ Retinal dystrophy with dysfunction of the inner retina and ganglion cell abnormalities. In: Orphanet (Rare Disease Database).
- ↑ Retinal dystrophy, severe, beginning in early childhood. In: Orphanet (Rare Disease Database).
- ↑ Retinal dystrophy, onset late. In: Orphanet (Rare Disease Database).
- ↑ Retinal dystrophy type Bothnia. In: Orphanet (Rare Disease Database).
- ^ Oguchi disease. In: Orphanet (Rare Disease Database).
- ↑ Pigmented paravenous retinochoroidal atrophy. In: Orphanet (Rare Disease Database).
- ↑ Progressive retinal dystrophy due to retinol transport defect. In: Orphanet (Rare Disease Database).
- ^ Retinal dysplasia, X-linked. In: Orphanet (Rare Disease Database).
- ↑ Retinal vasculopathy and cerebral leukoencephalopathy. In: Orphanet (Rare Disease Database).
- ^ Revesz syndrome. In: Orphanet (Rare Disease Database).
- ↑ X-linked intellectual disability-spasticity of the extremities-retinal dystrophy-diabetes insipidus syndrome. In: Orphanet (Rare Disease Database).
- ↑ Suppository deficiency trichromatism. In: Orphanet (Rare Disease Database).
- ↑ cone dystrophy with supernormal rod-B-waves. In: Orphanet (Rare Disease Database).
- ↑ Cerebellar-retinal degeneration, infantile. In: Orphanet (Rare Disease Database).