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Achondrogenesis is a rare type of growth hormone deficiency in which there is a defect in the development of bone and cartilage.


Achondrogenesis is inherited, which means it is passed down through families.

Some types are known to be recessive, meaning both parents carry the defective gene and the chance for a subsequent child to be affected is about 25%.

  • Very short trunk, arms, legs and neck
  • Head appears large in relation to the trunk
  • Small lower jaw
  • Narrow chest
Signs and tests

X-rays show bone problems associated with the condition.

Support Groups

Expectations (prognosis)

The outcome is generally very poor. Many infants with achondrogenesis are stillborn or die shortly after birth because of breathing problems related to the abnormally small chest.

Calling your health care provider

This condition is often diagnosed on the first examination of an infant.


This condition is often fatal early in life.


There is no current therapy. Talk to your doctor about care decisions.

Genetic counseling may be appropriate.


Review Date: 8/2/2009
Reviewed By: Neil K. Kaneshiro, MD, MHA, Clinical Assistant Professor of Pediatrics, University of Washington School of Medicine. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.
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