Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

Peters anomaly

Peters anomaly (PA) is a congenital corneal opacity disorder characterized by a central corneal leukoma that obstructs the pupil leading to visual loss as well as absence of the posterior corneal stroma and Descemet membrane.

Esotropia

A form of strabismus with one or both eyes turned inward ('crossed') to a relatively severe degree, usually defined as 10 diopters or more.

Total: 1

(per page)

PMID (PMCID)
27230591	FEMALE	Infant, Newborn
	Unilateral persistent fetal vasculature coexisting with anterior segment dysgenesia.
	Canizares B, Yago I, Pinero A, Ruiz M. Arch Soc Esp Oftalmol. 2017;92(1):40-43.
	A case is presented of a 4 week-old female neonate with Peters anomaly (PA) and unilateral persistent foetal vasculature (PFV) referred to our centre due to esotropia.