U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Search results

Items: 2

1.

Persistent hyperplastic primary vitreous, autosomal recessive

Persistent hyperplastic primary vitreous (PHPV), also termed 'persistent fetal vasculature,' is a developmental malformation of the eye in which the primary vitreous fails to regress in utero, resulting in the presence of a retrolental fibrovascular membrane with persistence of the posterior portion of the tunica vasculosa lentis and hyaloid artery. This abnormality is usually unilateral and associated with microphthalmia, cataract, glaucoma, and congenital retinal nonattachment (see Haddad et al., 1978; Khaliq et al., 2001; Prasov et al., 2012). PHPV shares phenotypic overlap with Norrie disease (310600). Genetic Heterogeneity of Persistent Hyperplastic Primary Vitreous A dominant form of PHPV has been described (PHPVAD; 611308). [from OMIM]

MedGen UID:
370100
Concept ID:
C1969783
Disease or Syndrome
2.

Retinal nonattachment

Failure of attachment of the retina during development. [from HPO]

MedGen UID:
867205
Concept ID:
C4021563
Congenital Abnormality

Supplemental Content

Find related data

Search details

See more...

Recent activity