Ultrastructure of the eye in fetal type II glycogenosis (Pompe's disease).

Published

Journal Article

Type II glycogenosis is an autosomal recessive storage disease characterized by absence of the enzyme acid alpha-1,4-glucosidase. The eye of a 16 week fetus, aborted after diagnosis by amniocentesis, was studied by light and electron microscopy. Extensive deposits of lysosomal and cytoplasmic glycogen were present in virtually all ocular tissues examined, with the notable exception of pigment epithelia (iris and retina). The massive glycogen deposits present in this, the youngest case thus far examined histologically, emphasize the involvement of the fetus from its earliest stages and the importance of prenatal diagnosis.

Full Text

Duke Authors

Cited Authors

  • Pokorny, KS; Ritch, R; Friedman, AH; Desnick, RJ

Published Date

  • January 1, 1982

Published In

Volume / Issue

  • 22 / 1

Start / End Page

  • 25 - 31

PubMed ID

  • 6948796

Pubmed Central ID

  • 6948796

International Standard Serial Number (ISSN)

  • 0146-0404

Language

  • eng

Conference Location

  • United States