These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Congenital Stationary Night Blindness.
    Author: Tsang SH, Sharma T.
    Journal: Adv Exp Med Biol; 2018; 1085():61-64. PubMed ID: 30578486.
    Abstract:
    In congenital stationary night blindness (CSNB), there is a defect in rod photoreceptor signal transmission. This disorder of night vision is non-progressive. The most common inheritance pattern is X-linked, though autosomal recessive and autosomal dominant patterns have been described (Fig. 13.1). There is genetic heterogeneity within these types.
    [Abstract] [Full Text] [Related] [New Search]