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Pansynostosis

Known as: Sysnostosis of all cranial sutures 
Craniosynostosis of all calvarial sutures. [DDD:awilkie]
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Classification of Subtypes of Crouzon Syndrome Based on the Type of Vault Suture Synostosis.
BACKGROUND Patients with Crouzon syndrome develop various types of anatomic deformities due to different forms of… 
Review
2007
Review
2007
Pansynostosis: a review
IntroductionAlthough rare, pansynostoses are seen and treated by the craniofacial surgeon. To date, a single source that reviews… 
2007
2007
Expansion Cranioplasty with Jackscrew Distracters for Craniosynostosis and Intracranial Hypertension in Transplanted Osteopetrosis
Background: An 11-month-old boy with autosomal recessive infantile osteopetrosis presented, 7 months after bone marrow… 
2006
2006
Case Report of Optic Atrophy in Pansynostosis: An Unusual Presentation of Scalp Edema from Hair Braiding
Pansynostosis (fusion of all cranial sutures) and optic atrophy were found as incidental CT scan and ophthalmological findings in… 
2003
2003
Maxillary Volume Growth in Craniosynostosis
&NA; Craniosynostosis, and in particular, craniofacial dysostosis, exhibits abnormalities of the nasomaxillary complex in form… 
Review
2001
Review
2001
Results of Cranial Vault Reshaping
This study was designed to assess the outcome of cranial vault reshaping for correction of deformity of the skull and the upper… 
1999
1999
Mutation of FGFR2 (cys278phe) in craniolacunia and pansynostosis
Editor—Craniolacunia (“Luckenschadel”) describes rounded or finger-like defects of the inner table of the membranous portion of… 
1998
1998
Demineralized bone bandeau in a patient with kleeblattschädel skull deformity.
Management of complex craniofacial deformities in the neonatal setting can pose daunting reconstructive challenges due to the… 
1987
1987
Therapy for Severe Craniostenoses
The surgical treatment of extreme craniostenoses (Tessier 1967), such as pansynostosis, Crouzon’s or Apert’s syndrome, is not yet… 
1964
1964
[CASE OF SYSNOSTOSIS HUMERORADIALIS CONGENITA].
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