X-linked endothelial corneal dystrophy
X-linked endothelial corneal dystrophy | |
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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
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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 | ||||||||||||||||||
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Globe |
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Pathways |
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Eye infections | |||||||||||||||||||
Sex linkage: X-linked disorders | |||||||||||||||||||||
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