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Article

Severe oculocerebrocutaneous (Delleman) syndrome: overlap with Goldenhar anomaly.

American journal of medical genetics - 7 Jul 1998

McCandless S E, Robin N H

Abstract excerpt

Oculocerebrocutaneous syndrome (OCCS), or Delleman syndrome, is a multiple congenital anomaly syndrome characterized by orbital cysts, cerebral malformations, and focal dermal hypoplasia [Delleman and Oorthuys, 1981, Clin Genet 19:191-198; Delleman et al., 1984, Clin Genet 25:470-472]. Two previous reports presented children having what is suggested as the more severe form of the OCCS syndrome who also had...

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Identifiers

PMID: 9677067
DOI: 10.1002/(sici)1096-8628(19980707)78:3<282::aid-ajmg15>3.0.co;2-b

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