Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1954 1
1958 1
1976 1
1977 1
1978 1
1980 1
1981 1
1983 1
1984 6
1985 4
1986 8
1987 5
1988 1
1989 4
1990 2
1991 9
1992 4
1993 3
1994 5
1995 9
1996 13
1997 17
1998 8
1999 9
2000 9
2001 11
2002 15
2003 12
2004 17
2005 8
2006 17
2007 25
2008 18
2009 25
2010 30
2011 34
2012 34
2013 23
2014 28
2015 29
2016 26
2017 26
2018 20
2019 19
2020 22
2021 27
2022 21
2023 13
2024 3

Text availability

Article attribute

Article type

Publication date

Search Results

565 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Abnormality of the fontanelles or cranial sutures"
Page 1
Nonsyndromic Craniosynostosis.
Dempsey RF, Monson LA, Maricevich RS, Truong TA, Olarunnipa S, Lam SK, Dauser RC, Hollier LH Jr, Buchanan EP. Dempsey RF, et al. Clin Plast Surg. 2019 Apr;46(2):123-139. doi: 10.1016/j.cps.2018.11.001. Epub 2019 Jan 30. Clin Plast Surg. 2019. PMID: 30851746 Review.
Nonsyndromic craniosynostosis is significantly more common than syndromic craniosynostosis, affecting the sagittal, coronal, metopic, and lambdoid sutures in decreasing order of frequency. Nonsyndromic craniosynostosis is most frequently associated with only 1 fused suture …
Nonsyndromic craniosynostosis is significantly more common than syndromic craniosynostosis, affecting the sagittal, coronal, metopic, and la …
Subarachnomegaly-venous congestion of infancy.
Sainz LV, Schuhmann MU. Sainz LV, et al. Childs Nerv Syst. 2021 Nov;37(11):3455-3463. doi: 10.1007/s00381-021-05328-z. Epub 2021 Oct 23. Childs Nerv Syst. 2021. PMID: 34687332 Free PMC article. Review.
PURPOSE: Multiple names within the literature refer to a clinical picture affecting infants and consisting of a large or fast growing head circumference with enlarged cortical subarachnoid spaces (CSAS) while cranial sutures are open. This myriad of terms demonstrat …
PURPOSE: Multiple names within the literature refer to a clinical picture affecting infants and consisting of a large or fast growing head c …
Complex craniosynostosis.
Czerwinski M, Kolar JC, Fearon JA. Czerwinski M, et al. Plast Reconstr Surg. 2011 Oct;128(4):955-961. doi: 10.1097/PRS.0b013e3182268ca6. Plast Reconstr Surg. 2011. PMID: 21681124
RESULTS: Over an 18-year period, 858 patients underwent craniosynostosis correction, and 31 patients (3.6 percent) satisfied inclusion criteria. Average number of affected sutures was 2.9 (lambdoid, 36 percent; sagittal, 31 percent; coronal, 18 percent; metopic, 15 percent …
RESULTS: Over an 18-year period, 858 patients underwent craniosynostosis correction, and 31 patients (3.6 percent) satisfied inclusion crite …
Congenital hypothyroidism.
Rastogi MV, LaFranchi SH. Rastogi MV, et al. Orphanet J Rare Dis. 2010 Jun 10;5:17. doi: 10.1186/1750-1172-5-17. Orphanet J Rare Dis. 2010. PMID: 20537182 Free PMC article. Review.
Congenital hypothyroidism (CH) occurs in approximately 1:2,000 to 1:4,000 newborns. ...On examination, common signs include myxedematous facies, large fontanels, macroglossia, a distended abdomen with umbilical hernia, and hypotonia. ...
Congenital hypothyroidism (CH) occurs in approximately 1:2,000 to 1:4,000 newborns. ...On examination, common signs include myxedemat
Carpenter syndrome.
Hidestrand P, Vasconez H, Cottrill C. Hidestrand P, et al. J Craniofac Surg. 2009 Jan;20(1):254-6. doi: 10.1097/SCS.0b013e318184357a. J Craniofac Surg. 2009. PMID: 19165041
There are 3 common features in all of these syndromes: craniosynostosis (skull base abnormalities, with early fusion in different sutures), midface hypoplasia, and musculoskeletal abnormalities. ...The brachycephaly is caused by early fusion in the coronal, s …
There are 3 common features in all of these syndromes: craniosynostosis (skull base abnormalities, with early fusion in different …
Trigonocephaly.
Zanini SA, Paglioli Neto E, Viterbo F, da Costa AR, Tershakowec M. Zanini SA, et al. J Craniofac Surg. 1992 Sep;3(2):85-9. doi: 10.1097/00001665-199209000-00007. J Craniofac Surg. 1992. PMID: 1290788
Trigonocephaly has been described either as an isolated anomaly or as part of the clinical spectrum of some well-known syndromes. Treatment, complications, and prognosis are closely related to the manifestations of the associated anomalies. ...
Trigonocephaly has been described either as an isolated anomaly or as part of the clinical spectrum of some well-known syndromes. Treatment, …
A Genetic-Pathophysiological Framework for Craniosynostosis.
Twigg SR, Wilkie AO. Twigg SR, et al. Am J Hum Genet. 2015 Sep 3;97(3):359-77. doi: 10.1016/j.ajhg.2015.07.006. Am J Hum Genet. 2015. PMID: 26340332 Free PMC article. Review.
Craniosynostosis, the premature fusion of one or more cranial sutures of the skull, provides a paradigm for investigating the interplay of genetic and environmental factors leading to malformation. ...In parallel, however, we need a pathogenetic classification to de …
Craniosynostosis, the premature fusion of one or more cranial sutures of the skull, provides a paradigm for investigating the …
Squamosal Suture Synostosis: An Under-Recognized Phenomenon.
W Beiriger J, Zhu X, Bruce MK, Irgebay Z, Smetona J, Losee JE, Goldstein JA. W Beiriger J, et al. Cleft Palate Craniofac J. 2023 Oct;60(10):1267-1272. doi: 10.1177/10556656221100675. Epub 2022 May 20. Cleft Palate Craniofac J. 2023. PMID: 35593077 Review.
Thirty-two patients (68%) had concomitant craniosynostosis of other sutures, most commonly sagittal and coronal. Nine patients (19%) underwent surgery to correct cranial malformations-all these patients had multi-suture synostosis (P = 0.012). ...The significance of …
Thirty-two patients (68%) had concomitant craniosynostosis of other sutures, most commonly sagittal and coronal. Nine patients (19%) …
Hydrocephalus in children.
Rizvi R, Anjum Q. Rizvi R, et al. J Pak Med Assoc. 2005 Nov;55(11):502-7. J Pak Med Assoc. 2005. PMID: 16304873 Review.
Approximately 55% of all hydrocephalus are congenital. The etiology depends upon the age of the child. The clinical features are increase in the size of head, with wide anterior fontanelle, prominent scalp veins, sun-setting eyes, optic nerve atrophy, nystagmus and …
Approximately 55% of all hydrocephalus are congenital. The etiology depends upon the age of the child. The clinical features are incr …
565 results