Acropectorovertebral dysplasia

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Acropectorovertebral dysplasia or F Syndrome, a genetic locus, is a rare skeletal dysplasia characterized by the fusion of the carpal and Tarsal bones, with the complex anomalies of the fingers and toes (preaxial polydactyly of the hands and/or feet, syndactyly of fingers and toes, hypoplasia and dysgenesis of metatarsal bones).[1]

Estimation[edit]

It is estimated that there are fewer than 1000 people who have it in the United States.[1]

Symptoms[edit]

Symptoms appear usually as a newborn or during pregnancy.[1]

References[edit]

  1. ^ a b c "Acropectorovertebral dysplasia".