CONDITION REFERENCE
Liebenberg syndrome
Information from MedlinePlus Genetics about this condition and how it can be inherited.
About this condition
Liebenberg syndrome is a condition that is characterized by abnormal development of the elbows, wrists, and hands. Joint deformities (contractures) that limit the movement of these structures are common. The signs and symptoms and the severity of Liebenberg syndrome can vary among affected individuals.
In people with Liebenberg syndrome, the bones and tissues of the elbows typically resemble those of the knees, and the arm bones near the elbow are shaped more like related structures in the leg. These changes limit the range of motion in the elbows.
Individuals with Liebenberg syndrome may have bones in the wrists that are joined together (fused), resembling related structures in the ankles and heels. This fusion can cause the hand to bend permanently toward the thumb (radial deviation).
Abnormalities of the hands and fingers may also be seen in individuals with Liebenberg syndrome. The bones in the hand that connect the wrist to the fingers (metacarpals) tend to be longer than normal, resembling the bones in the foot that connect the ankle to the toes. People with Liebenberg syndrome typically have fingers that are short (brachydactyly). Some affected individuals have a little finger that is permanently bent (camptodactyly) or fingers that are fused together (syndactyly).
Individuals with Liebenberg syndrome typically have no other signs and symptoms that are related to this condition. The development of the legs and feet is not affected.
Inheritance
- Autosomal dominant
A condition can have several forms with different inheritance patterns. Each pattern may apply to a different gene or form of the condition.
Related genes
MedlinePlus lists these genes for this condition. Open a gene page to read any available ClinGen reviews and ClinVar records.
YOUR DNA FILE
What can your DNA file tell you?
Your DNA file only includes the positions your test checked and reported. Consumer DNA kits usually test selected positions. Sequencing files can also leave out positions that were not reported or where the test could not give a result.
A variant missing from your file does not mean you tested negative for it. A ClinVar classification applies to a particular variant and the condition or finding it was reported for. It does not apply to everyone with that gene. An uncertain finding cannot establish a diagnosis.
BioDecode reads supported DNA files on your computer. It cannot fill gaps in your test, diagnose a condition or replace clinical testing.
Sources and dates
The source information on this page last changed on 2026-09-18.
MedlinePlus Source details
Source release: Fri, 18 Sep 2026 05:17:13 GMT
Source publication: 2026-01-12
Source review: 2026-01
SHA-256: fdc8bd614310c12718379cef6569962e5d0e791cecabcc355b53a72816ac263a
About the library sources · Latest validated release · Record 5885b77c2826