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.

chromosome 4q21 deletion 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.

Imprimir

Resumen

The 4q21 microdeletion syndrome is a newly described syndrome associated with facial dysmorphism, progressive growth restriction, severe intellectual deficit and absent or severely delayed speech.

Sinónimos

  • 4q21 microdeletion syndrome
  • Del(4)(q21)
  • chromosome 4q21 deletion syndrome
  • chromosome 4q21 deletion syndrome, isolated cases
  • monosomy 4q214q21 microdeletion syndrome
  • Del(4)(q21)
  • chromosome 4q21 deletion syndrome
  • chromosome 4q21 deletion syndrome, isolated cases
  • monosomy 4q21