Symptoms
Individuals with Jeune syndrome have some physical characteristics in common:
A long, narrow, and abnormally small chest with reduced lung capacityShort arms and legs compared to the trunk and overall small stature (short-limbed dwarfism)Kidney lesions which may lead to kidney failure
Other symptoms which individuals with Jeune syndrome may have are:
Intestinal malabsorptionRetinal degenerationLiver problemsHeart and circulatory problems
Often, severe respiratory distress appears during early infancy. In other cases, breathing problems are less severe, and abnormalities of the kidneys or gastrointestinal system may predominate.
Diagnosis
Jeune syndrome is usually diagnosed at birth based on the chest deformity and short-limbed dwarfism. Severely affected infants will have respiratory distress. Milder cases may be diagnosed by chest X-ray.
Treatment
The most important area of medical care for an individual with Jeune syndrome is preventing and treating respiratory infections. Unfortunately, many infants and children with the syndrome die from respiratory failure brought on by a very small chest and repeated respiratory infections.
In some cases, enlarging the rib cage with chest reconstructive surgery has been successful in relieving respiratory distress. This surgery is difficult and risky and has been reserved for children with severe breathing difficulties.
Individuals with Jeune syndrome may also develop high blood pressure from kidney disease. Their kidneys may eventually fail, which is treated by dialysis or kidney transplantation.
Many individuals with Jeune syndrome who survive infancy eventually begin to have normal chest development.
Genetic Counseling
Jeune syndrome is an inherited autosomal recessive disorder. This means that both parents must be carriers of the defective gene in order for a child to inherit the syndrome. Thus, if parents give birth to an affected child, this means both are carriers, and that each subsequent child they have has a 25% chance of inheriting the syndrome.
Edited by Richard N. Fogoros, MD