FAQ

Cranial Fontanelles

Known as: Fontanels, Cranial, Cranial Fontanels, Cranial Fontanelle 
Any of six membrane-covered openings between the CRANIAL SUTURES in the incompletely ossified skull of the fetus or newborn infant. The fontanelles… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1977-2016
012319772016

Related topics

Related topics

7 relations
Blood supply aspectsMicrobiologicalphysiological aspects

Narrower (4)

Mastoid FontanelleSphenoidal FontanelleStructure of anterior fontanel of skullStructure of posterior fontanel of skull

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
Cranial Fontanelles
physiological aspects
Blood supply aspects
Structure of anterior fontanel of skull
Microbiological
Mastoid Fontanelle

Papers overview

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2016
2016
A new frontonasal dysplasia syndrome associated with deletion of the SIX2 gene.
The frontonasal dysplasias are a group of craniofacial phenotypes characterized by hypertelorism, nasal clefting, frontal bossing… (More)
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2016
2016
A new species of Ituglanis (Siluriformes: Trichomycteridae) from the Tocantins and Paranaíba river basins, central Brazil, with remarks on the systematics of the genus.
Ituglanis goya, new species, is described from the Paranaíba and Tocantins river drainages, central Brazil. This is the first… (More)
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2014
2014
A new species of Ituglanis from the Rio Xingu Basin, Brazil, and the evolution of pelvic fin loss in trichomycterid catfishes (Teleostei: Siluriformes: Trichomycteridae).
A new species of the trichomycterid catfish genus Ituglanis is described from the Rio Curuá, Rio Xingu basin, Rio Amazonas… (More)
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2009
2009
Orthodontic treatment in a patient with cleidocranial dysostosis.
Cleidocranial dysostosis is a rare congenital skeletal disorder, associated with clavicular hypoplasia or aplasia, delayed… (More)
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2005
2005
Characterization of a new syndrome that associates craniosynostosis, delayed fontanel closure, parietal foramina, imperforate anus, and skin eruption: CDAGS.
We describe the clinical characterization, molecular analyses, and genetic mapping of a distinct genetic condition characterized… (More)
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2002
2002
Familial primary hypertrophic osteoarthropathy in association with congenital cardiac disease.
It is rare to find congenital cardiac disease in association with familial primary hypertrophic osteoarthropathy. We have now… (More)
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1999
1999
Nucleated red blood cell count at birth as an index of perinatal brain damage.
OBJECTIVE The prognostic value of the nucleated red blood cell count at birth with respect to perinatal brain damage and neonatal… (More)
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1996
1996
Relationship between neonatal nucleated red blood cell counts and hypoxic-ischemic injury.
OBJECTIVE To determine if nucleated red blood cell counts(RBC) are different in infants who develop intraventricular hemorrhage… (More)
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1991
1991
Renal tubular dysgenesis and very large cranial fontanels in a family with acrocephalosyndactyly S.C. type.
We describe the first case of renal tubular dysgenesis in a newborn female who survived 15 days. The immunohistochemical and… (More)
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1987
1987
Animal model: skeletal anomalies in mice with cleidocranial dysplasia.
Cleidocranial dysplasia in mice, a radiation-induced skeletal mutation, showed striking homology with cleidocranial dysplasia in… (More)
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