Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare corneal dystrophy characterized by thickened, redundant sheets of basement membrane extending into the corneal epithelium, as well as intraepithelial lacunae filled with cellular debris, together presenting as a pattern of ''maps'', ''dots'', and ''fingerprints'' on slit-lamp examination. Patients may be asymptomatic or present with recurrent episodes of painful corneal erosions with variable visual impairment, typically beginning after the age of thirty. The condition is bilateral and may be inherited in an autosomal dominant manner. Disease data Classification Disease Synonyms Anterior basement membrane dystrophy Cogan microcystic epithelial dystrophy EBMD Map-dot-fingerprint dystrophy Anterior basement membrane dystrophy Cogan microcystic epithelial dystrophy EBMD Map-dot-fingerprint dystrophy ORPHA code 98956 OMIM code 121820 ICD10 code H18.5 ICD11 code - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl