Literature DB >> 15980644

Prenatal diagnosis of cloverleaf skull: watch the hands!

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.

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Year:  2005        PMID: 15980644     DOI: 10.1159/000085089

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN: 1015-3837            Impact factor:   2.587


  2 in total

Review 1.  Pfeiffer type 2 syndrome: review with updates on its genetics and molecular biology.

Authors:  Rabjot Rai; Joe Iwanaga; Graham Dupont; Rod J Oskouian; Marios Loukas; W Jerry Oakes; R Shane Tubbs
Journal:  Childs Nerv Syst       Date:  2019-06-21       Impact factor: 1.475

2.  Prenatal diagnosis of craniosynostosis: value of MR imaging.

Authors:  M Irsutti Fjørtoft; A Sevely; S Boetto; S Kessler; M F Sarramon; M Rolland
Journal:  Neuroradiology       Date:  2007-02-20       Impact factor: 2.804

  2 in total

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