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GENATLAS PHENOTYPE

last update : 21-11-2022

Symbol	PPPCD
Location	10q26.11
Name	punctiform and polychromatic pre-Descemet corneal dystrophy
Corresponding gene	PRDX3
Main clinical features	characterized by the presence of tiny round multicolored opacities in the posterior stroma of the cornea, immediately anterior to the Descemet membrane patients asymptomatic and no visual disturbance
Genetic determination	autosomal dominant
Function/system disorder	eye
Type	disease

Remark(s)