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Year Number of Results
1985 1
1989 1
1991 1
1993 1
2001 2
2002 1
2003 1
2007 1
2009 1
2010 1
2013 2
2015 1
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2018 1
2019 2
2020 1
2021 1
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20 results

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Page 1
Diagnosis and Management of Suture-Related Concerns of the Infant Skull.
Hersh DS, Bookland MJ, Hughes CD. Hersh DS, et al. Pediatr Clin North Am. 2021 Aug;68(4):727-742. doi: 10.1016/j.pcl.2021.04.002. Pediatr Clin North Am. 2021. PMID: 34247705 Review.
The cranial fontanelles and sutures have several benign variations, including most cases of "early" or "late" closure of the anterior fontanelle, bathrocephaly, overriding sutures, and benign metopic ridging. ...Gaining comfort with the physical examination of an in …
The cranial fontanelles and sutures have several benign variations, including most cases of "early" or "late" closure of the anterior …
Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation.
Jaruga A, Hordyjewska E, Kandzierski G, Tylzanowski P. Jaruga A, et al. Clin Genet. 2016 Nov;90(5):393-402. doi: 10.1111/cge.12812. Epub 2016 Jun 30. Clin Genet. 2016. PMID: 27272193 Review.
CCD is an autosomal skeletal disorder characterized by several features such as delayed closure of fontanels, dental abnormalities and hypoplastic clavicles. Here, we summarize recent knowledge about RUNX2 function, mutations and their phenotypic consequences in pat …
CCD is an autosomal skeletal disorder characterized by several features such as delayed closure of fontanels, dental abnormalities …
Cleidocranial Dysplasia: A Review of Clinical, Radiological, Genetic Implications and a Guidelines Proposal.
Farrow E, Nicot R, Wiss A, Laborde A, Ferri J. Farrow E, et al. J Craniofac Surg. 2018 Mar;29(2):382-389. doi: 10.1097/SCS.0000000000004200. J Craniofac Surg. 2018. PMID: 29189406 Review.
In this review, we aimed to depict the clinical, radiological, and genetic features of cleidocranial dysplasia (CCD) and to suggest management guidelines, based on our experience of 8 cases, with an emphasis given to dental complications.The most common craniofacial features of C …
In this review, we aimed to depict the clinical, radiological, and genetic features of cleidocranial dysplasia (CCD) and to suggest manageme …
Congenital hypothyroidism: recommendations of the Thyroid Department of the Brazilian Society of Endocrinology and Metabolism.
Maciel LM, Kimura ET, Nogueira CR, Mazeto GM, Magalhães PK, Nascimento ML, Nesi-França S, Vieira SE; Brazilian Society of Endocrinology and Metabolism. Maciel LM, et al. Arq Bras Endocrinol Metabol. 2013 Apr;57(3):184-92. doi: 10.1590/s0004-27302013000300004. Arq Bras Endocrinol Metabol. 2013. PMID: 23681264 English, Portuguese.
Congenital hypothyroidism (CH) is the most common congenital endocrine disorder, with an incidence of 1:2,000 to 1:4,000 live births and it is a leading preventable mental retardation. ...The most frequent symptoms and signs are prolonged neonatal jaundice, hoarse c …
Congenital hypothyroidism (CH) is the most common congenital endocrine disorder, with an incidence of 1:2,000 to 1:4,000 live …
A new view of the neonatal brain: clinical utility of supplemental neurologic US imaging windows.
Di Salvo DN. Di Salvo DN. Radiographics. 2001 Jul-Aug;21(4):943-55. doi: 10.1148/radiographics.21.4.g01jl14943. Radiographics. 2001. PMID: 11452069 Review.
Anterior fontanelle imaging has traditionally been the mainstay of neonatal cranial ultrasonography (US). ...Posterior fontanelle imaging allows improved detection of intraventricular hemorrhage. ...
Anterior fontanelle imaging has traditionally been the mainstay of neonatal cranial ultrasonography (US). ...Posterior fontanelle …
A new parameter for the management of positional plagiocephaly: the size of the anterior fontanelle matters.
Wendling-Keim DS, Macé Y, Lochbihler H, Dietz HG, Lehner M. Wendling-Keim DS, et al. Childs Nerv Syst. 2020 Feb;36(2):363-371. doi: 10.1007/s00381-019-04215-y. Epub 2019 Jun 17. Childs Nerv Syst. 2020. PMID: 31209640
Therefore, it was the goal of this study to compare the results of physiotherapy and helmet therapy and to investigate if the size of the anterior fontanelle can be used as an additional parameter for the indication of the helmet therapy. ...Sixty-eight patie …
Therefore, it was the goal of this study to compare the results of physiotherapy and helmet therapy and to investigate if the size of …
A review of Donnai-Barrow and facio-oculo-acoustico-renal (DB/FOAR) syndrome: clinical features and differential diagnosis.
Pober BR, Longoni M, Noonan KM. Pober BR, et al. Birth Defects Res A Clin Mol Teratol. 2009 Jan;85(1):76-81. doi: 10.1002/bdra.20534. Birth Defects Res A Clin Mol Teratol. 2009. PMID: 19089858 Free PMC article. Review.
These features include: agenesis of the corpus callosum, developmental delay, enlarged anterior fontanelle, high myopia, hypertelorism, proteinuria, and sensorineural hearing loss. Congenital diaphragmatic hernia and omphalocele are reported in only half of the pati …
These features include: agenesis of the corpus callosum, developmental delay, enlarged anterior fontanelle, high myopia, hyperteloris …
Hindbrain morphometry and choroid plexus position in differential diagnosis of posterior fossa cystic malformations.
Paladini D, Donarini G, Parodi S, Volpe G, Sglavo G, Fulcheri E. Paladini D, et al. Ultrasound Obstet Gynecol. 2019 Aug;54(2):207-214. doi: 10.1002/uog.20120. Ultrasound Obstet Gynecol. 2019. PMID: 30207001 Free article.
All included cases had good-quality three-dimensional (3D) volume datasets of the posterior fossa, acquired by transvaginal ultrasound through the posterior fontanelle. The midsagittal view of the posterior fossa was the reference view for the study. ...Finally, the positi …
All included cases had good-quality three-dimensional (3D) volume datasets of the posterior fossa, acquired by transvaginal ultrasound throu …
Further delineation of phenotype and genotype of Kenny-Caffey syndrome type 2 (phenotype and genotype of KCS type 2).
Chen X, Zou C. Chen X, et al. Mol Genet Genomic Med. 2024 Apr;12(4):e2433. doi: 10.1002/mgg3.2433. Mol Genet Genomic Med. 2024. PMID: 38591167 Free PMC article. Review.
BACKGROUND: Kenny-Caffey syndrome type 2 (KCS2) is an extremely rare inherited disorder characterized by proportionate short stature, skeletal defects, ocular and dental abnormalities, and transient hypocalcemia. It is caused by variants in FAM111A gene. ...Endocrinologic …
BACKGROUND: Kenny-Caffey syndrome type 2 (KCS2) is an extremely rare inherited disorder characterized by proportionate short stature, skelet …
Clinical and ultrasonographic criteria for using ventriculoperitoneal shunts in newborns with myelomeningocele.
Melo JR, Pacheco P, Melo EN, Vasconcellos Â, Passos RK. Melo JR, et al. Arq Neuropsiquiatr. 2015 Sep;73(9):759-63. doi: 10.1590/0004-282X20150110. Arq Neuropsiquiatr. 2015. PMID: 26352494 Free article.
Parameters used to guide the indication of VP shunts included measurement of head circumference (HC), evaluation of fontanels, and measurement of lateral ventricular atrium (LVA) width by transcranial ultrasonography.Results 43 children were included in the analysis, of wh …
Parameters used to guide the indication of VP shunts included measurement of head circumference (HC), evaluation of fontanels, and me …
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