Saethre-Chotzen syndrome

Last revised by Yusra Sheikh on 2 Dec 2019

Saethre-Chotzen syndrome (also known as type III acrocephalosyndactyly) is characterized by limb and skull abnormalities.

It is the most common craniosynostosis syndrome and affects 1:25 - 50,000 individuals.

Males and females are equally affected.

The spectrum of observed clinical features include

It is thought to be due to mutations in the TWIST1 (twist transcription factor 1) gene located on chromosome 7p21 2. The condition is inherited in an autosomal dominant pattern.

It was first described by two psychiatrists, one Norwegian, Haakon Saethre and, the other German, F Chotzen, in 1931 and 1932 respectively 1.

Consider other forms of acrocephalosyndactyly such as

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