Prenatal ultrasound diagnosis of a case of Pfeiffer syndrome without cloverleaf skull and review of the literature-Reference-Cited by-同舟云学术

Prenatal ultrasound diagnosis of a case of Pfeiffer syndrome without cloverleaf skull and review of the literature

Published:2004 Issue:11 Volume:24 Page:918-922
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Nazzaro Alfredo,Monica Matteo Della,Lonardo Fortunato,Blasi Arturo Di,Baffico Maria,Baldi Maurizia,Nazzaro Giovanni,Placido Giuseppe De,Scarano Gioacchino

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference19 articles.

1. Trp290Cys mutation of the FGFR2 gene in a patient with severe Pfeiffer syndrome type 2

2. Using three-dimensional ultrasound to detect craniosynostosis in a fetus with Pfeiffer syndrome

3. Prenatal diagnosis of type 2 Pfeiffer syndrome

4. Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis

5. 2000. Craniosynostosis: Diagnosis, Evaluation and Management (2nd edn), Oxford University Press: New York.

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1. Type II Pfieffer misdiagnosed as Crouzon syndrome with additional features of supernumerary teeth and localized symmetrical gigantism: a case report;Journal of Medical Case Reports;2022-11-01

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3. Pfeiffer syndrome in an adult with previous surgical correction: A case report of CT findings;Radiology Case Reports;2021-09

4. Radiological Investigations of Craniofacial Malformations;Fundamentals of Craniofacial Malformations;2021

5. Apert syndrome: A case report of prenatal ultrasound, postmortem cranial CT , and molecular genetic analysis;Journal of Clinical Ultrasound;2020-09-21