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2004, Clinics in developmental medicine, ISBN 1898683360, Volume no. 163, xv, 421
Book
Child's Nervous System, ISSN 0256-7040, 01/2014, Volume 30, Issue 1, pp. 161 - 164
For patients with craniosynostosis, there is no single procedure available for reconstructing a normal cranial shape, regardless of the type of deformity. To... 
Craniosynostosis
Journal Article
World Neurosurgery, ISSN 1878-8750, 08/2019
Journal Article
The Antley-Bixler syndrome: Two new cases, 12/2001
The Antley-Bixler syndrome is a rare multiple congenital anomaly with a high mortality rate. The characteristic manifestations include craniosynostosis,... 
Craniosynostosis, radiohumeral synostosis, arachnodactyl, mid face hypoplasia
Journal
American Journal of Medical Genetics Part A, ISSN 1552-4825, 11/2018, Volume 176, Issue 11, pp. 2522 - 2522
Journal Article
Plastic and reconstructive surgery, ISSN 0032-1052, 06/2018, Volume 141, Issue 6, pp. 1508 - 1516
Occurring once in every 2000 live births, craniosynostosis is one of the most frequent congenital anomalies encountered by the craniofacial surgeon. Syndromic... 
SURGERY | AUTISM | DE-NOVO MUTATIONS | AUTOSOMAL-DOMINANT CRANIOSYNOSTOSIS | CONGENITAL HEART-DISEASE | GROWTH-FACTOR RECEPTOR-2 | PFEIFFER-SYNDROME | CORONAL CRANIOSYNOSTOSIS | CROUZON-SYNDROME | SPECTRUM | SAGITTAL CRANIOSYNOSTOSIS
Journal Article
Wiley Interdisciplinary Reviews, ISSN 1759-7684, 07/2016, Volume 5, Issue 4, pp. ii - ii
  The inside cover image, by Joan T. Richtsmeier et al., is based on the Advanced Review Understanding craniosynostosis as a growth disorder, DOI:... 
Layouts | Craniosynostosis
Journal Article
Laryngoscope, ISSN 0023-852X, 2018
1) Characterize the spectrum of airway anomalies in patients with craniosynostosis, and 2) identify clinical characteristics of these patients that may be... 
airway | Craniosynostosis | syndromic | craniofacial | pediatric
Journal Article
World Neurosurgery, ISSN 1878-8750, 11/2019, Volume 131, pp. 200 - 206
Craniosynostosis has a known association with rickets. Because of abnormal bone development and a tendency for patients with rickets to present at an older age... 
Rickets | Distraction osteogenesis | Pediatric | Craniosynostosis
Journal Article
Plastic and reconstructive surgery, ISSN 0032-1052, 06/2018, Volume 141, Issue 6, pp. 1474 - 1482
Background: Although studies have analyzed quality of life in children with nonsyndromic craniosynostosis, to date nobody has investigated long-term quality of... 
UNITED-STATES | SURGERY | SINGLE-SUTURE CRANIOSYNOSTOSIS | MANAGEMENT | PERSPECTIVE | SYNDROMIC CRANIOSYNOSTOSIS | FOLLOW-UP | OUTCOMES | SAGITTAL CRANIOSYNOSTOSIS | INTRACRANIAL-PRESSURE | CHILDREN
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 04/2017, Volume 54, Issue 4, pp. 260 - 268
Journal Article
Plastic and Reconstructive Surgery, ISSN 0032-1052, 09/2019, Volume 144, Issue 3, pp. 446e - 452e
This study aimed to detect the ability of pattern visual evoked potentials to detect visual pathway dysfunction in a cohort of patients with craniosynostosis... 
SURGERY | COMPLEX CRANIOSYNOSTOSIS | SAGITTAL SYNOSTOSIS | SYNDROMIC CRANIOSYNOSTOSIS | SINGLE-SUTURE | PAPILLEDEMA | CHILDREN
Journal Article
Cerebral hemiatrophy associated with hematological and developmental disorders, 07/2004
The etiology of cerebral hemiatrophy may be congenital or acquired. Trauma, infection, vascular abnormality, ischemic and hemorrhagic conditions may be the... 
Neurology | Pediatrics | cerebral hemiatrophy, thalassemia major, leukemia, craniosynostosis. pn04034
Journal
Current Opinion in Pediatrics, ISSN 1040-8703, 12/2017, Volume 29, Issue 6, pp. 622 - 628
Purpose of reviewWhen providing accurate clinical diagnosis and genetic counseling in craniosynostosis, the challenge is heightened by knowledge that etiology... 
exome sequencing | CDC45 | SMO | SMAD6 | SELFISH SPERMATOGONIAL SELECTION | NONSYNDROMIC SAGITTAL CRANIOSYNOSTOSIS | CURRY-JONES SYNDROME | CREST-MESODERM BOUNDARY | SYNDROMIC CRANIOSYNOSTOSIS | PEDIATRICS | CRANIOFACIAL SURGERY | CORONAL CRANIOSYNOSTOSIS | WHOLE GENOME | MUENKE SYNDROME | BONE DYSPLASIA-FGFR2 TYPE | Exome sequencing
Journal Article