Acropectorovertebral dysplasia
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]