X-linked endothelial corneal dystrophy

From Self-sufficiency

Revision as of 00:50, 7 October 2009 by Captain-n00dle (Talk) (added navbox)

(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

X-linked endothelial corneal dystrophy
Classification and external resources
OMIM	300779

X-linked endothelial corneal dystrophy (XECD) is a rare form of human corneal dystrophy described first in 2006.^[1] It is manifested as corneal clouding in the form of a ground glass, milky corneal tissue, and moon crater-like changes of corneal endothelium.

References

Cite error: Invalid <references> tag; parameter "group" is allowed only.

Use <references />, or <references group="..." />

Types of human corneal dystrophy

Epithelial and Subepithelial

Epithelial basement membrane dystrophy (OMIM 121820), called a corneal dystrophy but in reality this condition is not inherited in the majority of cases, representing a non-specific reaction to a variety of corneal insults. · Subepithelial mucinous corneal dystrophy · Meesmann juvenile epithelial corneal dystrophy (MECD, Stocker-Holt dystrophy, OMIM 122100) · Lisch epithelial dystrophy · Gelatinous drop-like corneal dystrophy

Bowman layer

Reis-Bucklers corneal dystrophy (CDB1) aka. Granular corneal dystrophy type III · Thiel-Behnke dystrophy (CDB2)

Stroma

Lattice corneal dystrophy type I · Lattice corneal dystrophy type II · Granular corneal dystrophy type I · Granular corneal dystrophy type II · Also Granular corneal dystrophy type III see Reis-Bucklers corneal dystrophy above · Macular corneal dystrophy · Schnyder corneal dystrophy · Congenital stromal dystrophy (CSCD) · Fleck dystrophy · Posterior amorphous corneal dystrophy

Descemet membrane and Endothelial

Fuchs' dystrophy · Posterior polymorphous dystrophy type 1 · Posterior polymorphous dystrophy type 2 · Posterior polymorphous dystrophy type 3 · Congenital endothelial dystrophy type 1 (CHED1) · Congenital endothelial dystrophy type 2 (CHED2) · X-linked endothelial corneal dystrophy

M: EYE

anat(g, a, p)/phys/devp/cell

noco/cong/tumr, epon

proc, drug(S1A/1E/1F/1L)

Eye disease · pathology of the eye (H00-H59, 360-379)

Adnexa

eyelid: inflammation (Stye, Chalazion, Blepharitis) · Entropion · Ectropion · Lagophthalmos · Blepharochalasis · Ptosis · Blepharophimosis · Xanthelasma · eyelash (Trichiasis, Madarosis)

lacrimal system: Dacryoadenitis · Epiphora · Dacryocystitis · Xerophthalmia

orbit: Exophthalmos · Enophthalmos · Orbital cellulitis · Periorbital cellulitis

conjunctiva: Conjunctivitis (Allergic conjunctivitis) · Pterygium · Pinguecula · Subconjunctival hemorrhage

Globe

Fibrous tunic

sclera: Scleritis
cornea: Keratitis (Herpetic keratitis, Acanthamoeba keratitis, Fungal keratitis) · Corneal ulcer · Photokeratitis · Thygeson's superficial punctate keratopathy · Corneal dystrophy (Fuchs', Meesmann) · Keratoconus · Keratoconjunctivitis sicca · Keratoconjunctivitis · Corneal neovascularization · Kayser-Fleischer ring · Arcus senilis · Band keratopathy

Vascular tunic

Iris and ciliary body	Iritis · Uveitis (Intermediate uveitis) · Iridocyclitis · Hyphema · Rubeosis iridis · Persistent pupillary membrane · Iridodialysis · Synechia
Choroid	Choroideremia · Choroiditis (Chorioretinitis)

Lens

Cataract · Aphakia · Ectopia lentis

Retina

Retinitis (Chorioretinitis, Cytomegalovirus retinitis) · Retinal detachment · Retinoschisis · Ocular ischemic syndrome/Central retinal vein occlusion · Retinopathy (Bietti's crystalline dystrophy, Coats disease, Diabetic retinopathy, Hypertensive retinopathy, Retinopathy of prematurity) · Macular degeneration · Retinitis pigmentosa · Retinal haemorrhage · Central serous retinopathy · Macular edema · Epiretinal membrane · Macular pucker · Vitelliform macular dystrophy · Leber's congenital amaurosis · Birdshot chorioretinopathy

Other

Glaucoma/Ocular hypertension · Floater · Leber's hereditary optic neuropathy · Red eye · Keratomycosis · Phthisis bulbi

Pathways

Optic nerve and
visual pathways

Optic neuritis · Papilledema · Optic atrophy · Leber's hereditary optic neuropathy · Dominant optic atrophy · Optic disc drusen · Glaucoma · Toxic and nutritional optic neuropathy · Anterior ischemic optic neuropathy

Ocular muscles,
binocular movement,
accommodation

Paralytic strabismus	Ophthalmoparesis · Progressive external ophthalmoplegia · Palsy (III, IV, VI) · Kearns-Sayre syndrome
Other strabismus	Esotropia/Exotropia · Hypertropia · Heterophoria (Esophoria, Exophoria) · Brown's syndrome · Duane syndrome
Other binocular	Conjugate gaze palsy · Convergence insufficiency · Internuclear ophthalmoplegia · One and a half syndrome

Refraction

Refractive error: Hyperopia/Myopia · Astigmatism · Anisometropia/Aniseikonia · Presbyopia

Visual disturbances
and blindness

Amblyopia · Leber's congenital amaurosis · Subjective (Asthenopia, Hemeralopia, Photophobia, Scintillating scotoma) · Diplopia · Scotoma · Anopsia (Binasal hemianopsia, Bitemporal hemianopsia, Homonymous hemianopsia, Quadrantanopia) · Color blindness (Achromatopsia, Dichromacy, Monochromacy) · Nyctalopia (Oguchi disease) · Blindness/Low vision

Pupil

Anisocoria · Argyll Robertson pupil · Marcus Gunn pupil · Adie syndrome · Miosis · Mydriasis · Cycloplegia

Other

Nystagmus

Eye infections

Trachoma · Onchocerciasis

M: EYE

anat(g, a, p)/phys/devp/cell

noco/cong/tumr, epon

proc, drug(S1A/1E/1F/1L)

Sex linkage: X-linked disorders

X-linked recessive
Immune	Chronic granulomatous disease (CYBB) · Wiskott-Aldrich syndrome · X-linked severe combined immunodeficiency · X-linked agammaglobulinemia · Hyper-IgM syndrome type 1 · IPEX · X-linked lymphoproliferative disease
Hematologic	Haemophilia A · Haemophilia B · X-linked sideroblastic anemia
Endocrine	Androgen insensitivity syndrome/Kennedy disease · KAL1 Kallmann syndrome · X-linked adrenal hypoplasia congenita
Metabolic	amino acid: Ornithine transcarbamylase deficiency · Oculocerebrorenal syndrome dyslipidemia: Adrenoleukodystrophy carbohydrate metabolism: Glucose-6-phosphate dehydrogenase deficiency · Pyruvate dehydrogenase deficiency · Danon disease/glycogen storage disease Type IIb lipid storage disorder: Fabry's disease mucopolysaccharidosis: Hunter syndrome purine-pyrimidine metabolism: Lesch-Nyhan syndrome mineral: Menkes disease/Occipital horn syndrome
Nervous system	X-Linked mental retardation: Coffin-Lowry syndrome · MASA syndrome · X-linked alpha thalassemia mental retardation syndrome · Siderius X-linked mental retardation syndrome eye disorders: Color blindness (red and green, but not blue) · Ocular albinism (1) · Norrie disease · Choroideremia other: Charcot-Marie-Tooth disease (CMTX2-3) · Pelizaeus-Merzbacher disease · SMAX2
Skin and related tissue	Dyskeratosis congenita · Hypohidrotic ectodermal dysplasia (EDA) · X-linked ichthyosis · X-linked endothelial corneal dystrophy
Neuromuscular	Becker's muscular dystrophy/Duchenne · Centronuclear myopathy (MTM1) · Conradi-Hünermann syndrome
Urologic	Alport syndrome · Dent's disease · X-linked nephrogenic diabetes insipidus
No primary system	Barth syndrome · McLeod syndrome · Smith-Fineman-Myers syndrome · Simpson-Golabi-Behmel syndrome

X-linked dominant
X-linked hypophosphatemia · Focal dermal hypoplasia · Fragile X syndrome · Aicardi syndrome · Incontinentia pigmenti · Rett syndrome · CHILD syndrome · Lujan-Fryns syndrome

ru:Х-связанная эндотелиальная дистрофия роговицы

↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.

Retrieved from "http://ssf.f15ijp.com/wiki/index.php?title=X-linked_endothelial_corneal_dystrophy&oldid=26523"

Categories:

X-linked endothelial corneal dystrophy

References

Navigation menu

Views

Personal tools

Navigation

Search

Tools

adverts