Lambdoidal synostosis in dizygotic twins with a family history of an undiagnosed connective tissue disorder

Author:

Watson Caroline C.,Griessenauer Christoph J.,Tubbs R. Shane,Johnston James M.

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference19 articles.

1. Bradley JP, Shahinian H, Levine JP, Rowe N, Longaker MT (2000) Growth restriction of cranial sutures in the fetal lamb causes deformational changes, not craniosynostosis. Plast Reconstr Surg 105:2416–2423

2. Cohen MM Jr (1996) Lambdoid synostosis is an overdiagnosed condition. Am J Med Genet 61:98–99

3. Cohen MM Jr (2000) Craniofacial disorders caused by mutations in homeobox genes MSX1 and MSX2. J Craniofac Genet Dev Biol 20:19–25

4. Cruysberg JR, van Ravenswaaij-Arts CM, Pinckers A, Roddi R, Brunner HG (1999) Craniosynostosis associated with ectopia lentis in monozygotic twin sisters. Am J Med Genet 82:201–205

5. Dong J, Bu J, Du W, Li Y, Jia Y, Li J, Meng X, Yuan M, Peng X, Zhou A, Wang L (2012) A new novel mutation in FBN1 causes autosomal dominant Marfan syndrome in a Chinese family. Mol Vis 18:81–86

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1. Lambdoidal Craniosynostosis;Smith's Recognizable Patterns of Human Deformation;2025

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