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What is the disease CGF?

Published in Medical Condition 1 min read

Congenital Generalized Fibromatosis (CGF) is a rare disease characterized by multiple fibromatous tumors present at birth.

Understanding Congenital Generalized Fibromatosis (CGF)

CGF is a condition where numerous non-cancerous (fibromatous) tumors are present in a newborn. Let's delve deeper:

  • Presence at Birth: A key characteristic is that these tumors are already present when the baby is born.
  • Fibromatous Tumors: These are growths made up of fibrous tissue. They are typically benign (non-cancerous).
  • Infancy Progression: According to the reference, these tumors often proliferate and grow during infancy.
  • Spontaneous Regression: If the patient survives, the tumors may spontaneously regress (shrink or disappear) over time. This is a distinctive feature of CGF.

Key Aspects Summarized

Feature Description
Name Congenital Generalized Fibromatosis (CGF)
Nature Rare disease
Tumors Multiple fibromatous tumors
Onset Present at birth
Tumor Behavior Proliferation and growth during infancy
Potential Outcome Spontaneous regression (if the patient survives)