Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome

What is Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome?

Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome is a rare developmental defect of the eye characterized by bilateral microcornea, posterior megalolenticonus, persistent fetal vasculature (extending from the posterior pole of the lens to the optic disc) and posterior chorioretinal coloboma.

Other condition names

  • MPPC syndrome

Inheritance type

Unknown

Prevalence

  • Worldwide: <1 in 1,000 000

Age of Onset

  • Infancy
  • Neonatal
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