Orphanet: Peters anomaly

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Peters anomaly

Disease definition

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.

ORPHA:708

Classification level: Disorder

Synonym(s):
- Peters congenital glaucoma
Prevalence: <1 / 1 000 000
Inheritance: Autosomal dominant or Autosomal recessive
Age of onset: Infancy, Neonatal
ICD-10: Q13.4
ICD-11: 9C61.42
OMIM: 604229 612968
UMLS: -
MeSH: C537884
GARD: 7377
MedDRA: 10059202

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Peters anomaly

ORPHA:708

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