Y-craniosynostosis by premature fusion of the metopic and coronal sutures: A new nosological entity or a variety of Saethre-Chotzen syndrome?

Author:

di Rocco Federico1,Benoit Alexandra1,Vigneron Jacqueline2,Segura Pascale Bach3,Klein Olivier4,Collet Corinne5,Arnaud Eric1

Affiliation:

1. Unité de Chirurgie Craniofaciale, Service de Neurochirurgie, Centre de Référence National Dysostoses Crâniofaciales, Hôpital Necker; Paris France

2. UF de génétique médicale, Maternité régionale; CHU deNancy France

3. Service de radiologie, CHUdeNancy; France

4. Service de Neurochirurgie pédiatrique; CHU deNancy France

5. Unité Fonctionnelle de Génétique Moléculaire, Service de Biochimie et Biologie Moléculaire, Pôle B2P, Hôpital Lariboisière; Paris France

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Saethre-Chotzen syndrome: Case report and literature review;Dental and Medical Problems;2018-06-30

2. Increased detection of genetic loci associated with risk predictors of osteoporotic fracture using a pleiotropic cFDR method;Bone;2017-06

3. Genetic advances in craniosynostosis;American Journal of Medical Genetics Part A;2017-02-04

4. Saethre-Chotzen Syndrome;Atlas of Genetic Diagnosis and Counseling;2017

5. Craniosynostosis Syndromes: Genetics to Imaging;Journal of Pediatric Neuroradiology;2016-10-03

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