Pfeiffer R A, Rinnert S, Popp R, Röckelein G
Institut für Humangenetik, Friedrich-Alexander Universität Erlangen-Nürnberg, Germany.
Am J Med Genet. 1996 May 3;63(1):175-6. doi: 10.1002/(SICI)1096-8628(19960503)63:1<175::AID-AJMG30>3.0.CO;2-J.
We report on a male infant with an unusual type of acrocephalosyndactyly presenting with unilateral coronal craniosynostosis, cutaneous syndactyly of toes 2 and 3, loss of distal triradii, and transverse alignment of dermal ridges of the palm suggesting syndactyly, atresia of the proximal jejunum, and anal stenosis.