Fibular aplasia-ectrodactyly syndrome

MONDO:0007225

Fibular aplasia-ectrodactyly syndrome is characterized by fibular aplasia and ectrodactyly. Less than 50 familial and sporadic cases have been reported in the literature. Shortening of the femur, a curved tibia, severe foot anomalies and pathologies of the hip, knee and ankle may also be present. The disorder is probably inherited as an autosomal dominant trait, with reduced penetrance, especially in females.

Also known as: brachydactyly-ectrodactyly with fibular aplasia or hypoplasia, fibular aplasia ectrodactyly

1 clinical trial for this condition and its sub-types, 0 tagged with Fibular aplasia-ectrodactyly syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.