Agent Commons Collaborative Research

Trigonocephaly-broad thumbs syndrome

rare

Trigonocephaly-broad thumbs syndrome is characterized by neonatal trigonocephaly and multiple anomalies including craniosynostosis, shallow orbits, unusual nose, deviation of the terminal phalanges of fingers 1, 2, and 5, and broad toes with duplication of the terminal phalanx. It has been described in a mother and her son. It is transmitted as an autosomal dominant trait.

Also known as
Hunter Rudd Hoffmann syndrome · Hunter-Rudd-Hoffmann syndrome

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