Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

The Hallermann-Streiff syndrome.

G A De Wilde1, F M Meire

  • 1Department of Ophthalmology, University Hospital, Gent, Belgium.

Bulletin De La Societe Belge D'Ophtalmologie
|January 1, 1991
PubMed
Summary

Hallermann-Streiff syndrome presents with systemic and eye issues like congenital cataracts and microphthalmia. This case report discusses its differential diagnosis for better understanding.

Related Experiment Videos

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Chiasmal misrouting and foveal hypoplasia without albinism.

The British journal of ophthalmology·2006
Same author

Ophthalmologic and systemic features of the Alström syndrome: report of 9 cases.

Bulletin de la Societe belge d'ophtalmologie·2001
Same author

Use of mitomycin C and r-tPA for the management of conjunctival membrane and cataracts in a child with conjunctivitis lignosa.

The British journal of ophthalmology·2001
Same author

Thiamine-responsive megaloblastic anemia syndrome (TRMA) with cone-rod dystrophy.

Ophthalmic genetics·2001
Same author

Lenticonus.

Bulletin de la Societe belge d'ophtalmologie·2000
Same author

Retinopathy following measles, mumps, and rubella vaccination in an immuno-incompetent girl.

International ophthalmology·2000

Area of Science:

  • Ophthalmology
  • Genetics
  • Pediatrics

Background:

  • Hallermann-Streiff syndrome is a rare genetic disorder.
  • It is characterized by distinctive facial dysmorphisms and congenital anomalies.
  • Ocular manifestations, including congenital cataract and microphthalmia, are key features.