Additional Resources

Section

NORD rare disease drug development ad.
NORD State Resource Center Sidebar photo.

Get Information about a Rare Disease

Use the form below to explore NORD's comprehensive rare disease database. Search for detailed information on rare diseases, including NORD's authoritative Rare Disease Reports and data from other reliable sources.
* = NORD Rare Disease Report

Interested in exploring the database in detail?
Click here to explore the database in alphabetical order.

laryngo-onycho-cutaneous syndrome

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

Print

Disease Overview

LOC syndrome is a subtype of junctional epidermolysis bullosa (JEB) characterized by an altered cry in the neonatal period and by aberrant production of granulation tissue in particular affecting the upper airway tract, conjunctiva and periungual/subungual sites.

Synonyms

  • LARYNGOONYCHOCUTANEOUS syndrome
  • LOC syndrome
  • LOCS
  • Shabbir syndrome
  • laryngeal and ocular granulation tissue in children from the Indian subcontinent syndrome
  • laryngo-onycho-cutaneous syndrome
  • logic syndromeLARYNGOONYCHOCUTANEOUS syndrome
  • LOC syndrome
  • LOCS
  • Shabbir syndrome
  • laryngeal and ocular granulation tissue in children from the Indian subcontinent syndrome
  • laryngo-onycho-cutaneous syndrome
  • logic syndrome
Sign Up for NORD News