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1. The clinical management of craniosynostosis
by Hayward, Richard
2004, Clinics in developmental medicine, ISBN 1898683360, Volume no. 163, xv, 421
Craniosynostoses
Book
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2. Twenty-five-years follow-up results of our total cranial reshaping abamboo-ware methoda
by Nakajima, Hideo and Sakamoto, Yoshiaki and Tamada, Ikkei
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
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3. Full Text Understanding craniofacial anomalies
: the etiopathogenesis of craniosynostoses and facial clefting
by Mooney, Mark P and Siegel, Michael I
2002, ISBN 047138724X
Skull | Cleft palate | Craniosynostoses | Genetic aspects | Face | Abnormalities
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4. Full Text Utility of Postoperative Fever Workup After Craniosynostosis Repair
by Field, Nicholas C and Raviv, Nataly and Adamo, Matthew A
World Neurosurgery, ISSN 1878-8750, 08/2019
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5. The Antley-Bixler syndrome: Two new cases
by Hosalkar, H. S and Shah, H. S and Gujar, P. S and Shaw, B. A
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
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6. Full Text Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. Am J Med Genet A. 2018 Feb;176(2):290‐300
by Clarke, CM and Fok, VT and Gustafson, JA and Smyth, MD and Timms, AE and Frazar, CD and Smith, JD and Birgfeld, CB and Lee, A and Ellenbogen, RG and Gruss, JS and Hopper, RA and Cunningham, ML
American Journal of Medical Genetics Part A, ISSN 1552-4825, 11/2018, Volume 176, Issue 11, pp. 2522 - 2522
Genes | Genetic aspects | Craniosynostosis
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7. Full Text Squamosal Craniosynostosis: Defining the Phenotype and Indications for Surgical Management
by Tadisina, Kashyap Komarraju and Lin, Alexander Y
Annals of Plastic Surgery, ISSN 0148-7043, 11/2017, Volume 79, Issue 5, pp. 458 - 466
BACKGROUNDSquamosal craniosynostosis is seldom reported in the craniofacial literature. Given that this is an uncommon diagnosis, phenotype and management... 
syndromic craniosynostosis | craniosynostosis | nonsyndromic craniosynostosis | squamosal suture | craniofacial surgery | cranial vault surgery | squamosal craniosynostosis | SURGERY | FUSION | RARE | CRANIAL VAULT | CONSTRAINT | BASE | ASYMMETRY | GROWTH | SUTURE CRANIOSYNOSTOSIS | SYNOSTOSIS | Severity of Illness Index | Prognosis | Risk Assessment | Humans | Craniosynostoses - surgery | Epithelial Cells - pathology | Infant | Male | Treatment Outcome | Rare Diseases | Craniosynostoses - therapy | Sampling Studies | Patient Selection | Craniosynostoses - diagnostic imaging | Phenotype | Observation - methods | Craniotomy - methods | Female | Retrospective Studies | Imaging, Three-Dimensional
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8. Full Text Genetics of Nonsyndromic Craniosynostosis
by Timberlake, Andrew T and Persing, John A
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
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9. Full Text Inside Cover Image, Volume 5, Issue 4
by Kevin Flaherty and Nandini Singh and Joan T Richtsmeier
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
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10. Full Text Impact of genetics on the diagnosis and clinical management of syndromic craniosynostoses
by Agochukwu, Nneamaka B and Solomon, Benjamin D and Muenke, Maximilian
Child's Nervous System, ISSN 0256-7040, 9/2012, Volume 28, Issue 9, pp. 1447 - 1463
More than 60 different mutations have been identified to be causal in syndromic forms of craniosynostosis. The majority of these mutations occur in the... 
Syndromic craniosynostoses | Neurosciences | Medicine & Public Health | Craniosynostosis | Diagnosis craniosynostosis | FGFR craniosynostosis | Neurosurgery | Craniosynostosis syndromes | Management craniosynostosis | SURGERY | MUENKE-SYNDROME | JACKSON-WEISS-SYNDROME | FRONTO-ORBITAL ADVANCEMENT | IDENTICAL MUTATIONS | PFEIFFER-SYNDROME | SAETHRE-CHOTZEN-SYNDROME | CLINICAL NEUROLOGY | HEARING-LOSS | APERT-SYNDROME | PEDIATRICS | CORONAL SYNOSTOSIS | CROUZON-SYNDROME | Acrocephalosyndactylia - history | Follow-Up Studies | Craniosynostoses - complications | Craniosynostoses - genetics | History, 20th Century | Humans | Craniosynostoses - diagnosis | Tomography, X-Ray Computed | Acrocephalosyndactylia - genetics | Mutation - genetics | Receptor, Fibroblast Growth Factor, Type 2 - genetics
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11. Full Text Airway anomalies in patients with craniosynostosis
by Mathews, Fasil and Shaffer, Amber D and Georg, Matthew W and Ford, Matthew D and Goldstein, Jesse A and Jabbour, Noel and Simons, Jeffrey P
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
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12. Full Text The Use of Distraction Osteogenesis in the Treatment of Rickets-Associated Craniosynostosis
by D'Agostino, Erin and Calnan, Daniel R and Whitson, Wesley and Stotland, Mitchell and Bauer, David F
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
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13. Full Text Muenke syndrome: Medical and surgical comorbidities and long‐term management
by Murali, Chaya N and McDonald‐McGinn, Donna M and Wenger, Tara Lynn and McDougall, Carey and Stroup, Bridget M and Sheppard, Sarah E and Taylor, Jesse and Bartlett, Scott P and Bhoj, Elizabeth J and Zackai, Elaine H and Santani, Avni
American Journal of Medical Genetics Part A, ISSN 1552-4825, 08/2019, Volume 179, Issue 8, pp. 1442 - 1450
Muenke syndrome (MIM #602849), the most common syndromic craniosynostosis, results from the recurrent pathogenic p.P250R variant in FGFR3 . Affected patients... 
Muenke syndrome | FGFR3 | reduced penetrance | variable expressivity | affected family members | related craniosynostosis | FGFR3-related craniosynostosis | PHENOTYPIC VARIABILITY | PRO250ARG MUTATION | EXPANSION | GROWTH | GENES | GENETICS & HEREDITY | CORONAL CRANIOSYNOSTOSIS | Autism | Medical research | Medical colleges | Comorbidity | Analysis | Medical genetics | Medicine, Experimental | Resource utilization | Craniosynostosis | Phenotypic variations | Dysostosis | Mutation | Management | Patients | Fibroblast growth factor receptors | Hearing loss
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14. Full Text Quality of Life in Adults with Nonsyndromic Craniosynostosis
by Mazzaferro, Daniel M and Naran, Sanjay and Wes, Ari M and Magee, Leanne and Taylor, Jesse A and Bartlett, Scott P
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
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15. Full Text Craniosynostosis
by Johnson, David and Wilkie, Andrew O. M
European Journal of Human Genetics, ISSN 1018-4813, 04/2011, Volume 19, Issue 4, pp. 369 - 376
Craniosynostosis, defined as the premature fusion of the cranial sutures, presents many challenges in classification and treatment. At least 20% of cases are... 
FGFR | craniosynostosis | TWIST | BIOCHEMISTRY & MOLECULAR BIOLOGY | FGFR2 MUTATIONS | CRANIOFRONTONASAL SYNDROME | SAETHRE-CHOTZEN-SYNDROME | GENETIC CONSIDERATIONS | SOMATIC MOSAICISM | NONSYNDROMIC CORONAL CRANIOSYNOSTOSIS | APERT-SYNDROME | MOUSE MODEL | GENETICS & HEREDITY | SYNDROMIC CRANIOSYNOSTOSIS | CROUZON-SYNDROME | Receptor, Fibroblast Growth Factor, Type 3 - genetics | Cranial Sutures | Ephrin-B1 - genetics | Tomography Scanners, X-Ray Computed | Risk Assessment | Craniosynostoses - genetics | Humans | Prenatal Diagnosis | Craniosynostoses - diagnosis | Male | Mutation - genetics | Receptor, Fibroblast Growth Factor, Type 1 - genetics | Genetic Counseling | Chromosome Aberrations | Twist-Related Protein 1 - genetics | Female | Nuclear Proteins - genetics | Child | Craniosynostoses - pathology | Receptor, Fibroblast Growth Factor, Type 2 - genetics | Craniosynostosis | Genes | Genetic analysis | Classification | Sutures | Genetics | Bones | Skull | Mutation | Diagnosis | Gene mapping | Eye protection | Chromosome aberrations | Practical Genetics
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16. Full Text Diagnostic value of exome and whole genome sequencing in craniosynostosis
by Miller, Kerry A and Twigg, Stephen R F and McGowan, Simon J and Phipps, Julie M and Fenwick, Aimée L and Johnson, David and Wall, Steven A and Noons, Peter and Rees, Katie E M and Tidey, Elizabeth A and Craft, Judith and Taylor, John and Taylor, Jenny C and Goos, Jacqueline A C and Swagemakers, Sigrid M A and Mathijssen, Irene M J and van der Spek, Peter J and Lord, Helen and Lester, Tracy and Abid, Noina and Cilliers, Deirdre and Hurst, Jane A and Morton, Jenny E V and Sweeney, Elizabeth and Weber, Astrid and Wilson, Louise C and Wilkie, Andrew O M
Journal of Medical Genetics, ISSN 0022-2593, 04/2017, Volume 54, Issue 4, pp. 260 - 268
BackgroundCraniosynostosis, the premature fusion of one or more cranial sutures, occurs in ∼1 in 2250 births, either in isolation or as part of a syndrome.... 
SHPRINTZEN-GOLDBERG SYNDROME | AUTOSOMAL-DOMINANT CRANIOSYNOSTOSIS | GENE | GENETICS & HEREDITY | CRANIOFRONTONASAL SYNDROME | GROWTH-FACTOR RECEPTOR-2 | SAETHRE-CHOTZEN SYNDROME | CORONAL CRANIOSYNOSTOSIS | CROUZON-SYNDROME | MUTATIONS | NOONAN-SYNDROME | Predictive Value of Tests | Exome - genetics | Genetic Testing | Craniosynostoses - genetics | Humans | Craniosynostoses - diagnosis | High-Throughput Nucleotide Sequencing | Mutation | Genome, Human | Neoplasm Proteins - genetics | Craniosynostoses - pathology | Craniosynostoses | Usage | Gene mutations | Genetic aspects | Diagnosis | Nucleotide sequencing | Research | Risk factors | DNA sequencing | Exome | whole genome sequencing | Actionable mutation | 1506 | Craniosynostosis | Developmental Defects
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17. Full Text Familial incidence and associated symptoms in a population of individuals with nonsyndromic craniosynostosis
by Greenwood, Jaclyn and Flodman, Pamela and Osann, Kathryn and Boyadjiev, Simeon A and Kimonis, Virginia
Genetics in Medicine, ISSN 1098-3600, 2014, Volume 16, Issue 4, pp. 302 - 310
Purpose: Craniosynostosis is a common cranial malformation occurring in 1 per 2,000-2,500 births. Isolated defects (nonsyndromic) occur in similar to 75% of... 
symptoms | nonsyndromic craniosynostosis | familial incidence | SINGLE-SUTURE CRANIOSYNOSTOSIS | RISK | PREVALENCE | NON-SYNDROMIC CRANIOSYNOSTOSIS | CHILDREN | NEURODEVELOPMENT | CLINICAL FINDINGS | GENETICS & HEREDITY | CORONAL SYNOSTOSIS | SAGITTAL CRANIOSYNOSTOSIS | LAMBDOID SYNOSTOSIS | Craniosynostoses - epidemiology | Humans | Risk Factors | Child, Preschool | Infant | Male | Cranial Sutures - pathology | Incidence | Young Adult | Phenotype | Craniosynostoses - classification | Health Surveys | Pedigree | Adolescent | Female | Child | Craniosynostoses - pathology
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18. Full Text Serial Visual Evoked Potentials in Patients with Craniosynostosis and Invasive Intracranial Pressure Monitoring
by Haredy, Mostafa M and Liasis, Alki and Fu, Valeria and Davis, Amani and Pollack, Ian F and Losee, Joseph E and Saied, Samia and Nischal, Ken K and Goldstein, Jesse A
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
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19. Cerebral hemiatrophy associated with hematological and developmental disorders
by Ünal, Özkan and Çaksen, Hüseyin and Kıymaz, Nejmi and Dilek, İmdat and Kayan, Mustafa and Anlar, Ömer
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
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20. Full Text Clinical genetics of craniosynostosis
by Wilkie, Andrew O.M and Johnson, David and Wall, Steven A
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
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