| Literature DB >> 15980644 |
Guillaume Gorincour1, Françoise Rypens, Andrée Grignon, Laurent Garel, Patricia Bortoluzzi, Luc Oligny, Emmanuelle Lemyre, Louise Duperron.
Abstract
Pfeiffer syndrome is an extremely rare autosomal-dominant condition whose prenatal diagnosis has only been reported 6 times, mainly on the basis of a fetal cloverleaf skull deformity. Three types have been described, each with a different prognosis. This case report stresses the need to thoroughly analyze the fetus and particularly the fetal hands in case of prenatal observation of a cloverleaf skull. The discovery of characteristic hand abnormalities allowed the early prenatal detection of type 2 Pfeiffer syndrome in our patient. (c) 2005 S. Karger AG, Basel.Entities:
Mesh:
Year: 2005 PMID: 15980644 DOI: 10.1159/000085089
Source DB: PubMed Journal: Fetal Diagn Ther ISSN: 1015-3837 Impact factor: 2.587