Relevant bibliographies by topics / Palate Cranial sutures

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Palate Cranial sutures'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Palate Cranial sutures.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Palate Cranial sutures"

1

Tedman, R. "Sex- and age-related variations in cranial measurements and suture closure in the Australian sea lion, Neophoca cinerea (Peron, 1816)." Australian Journal of Zoology 51, no. 5 (2003): 463. http://dx.doi.org/10.1071/zo02077.

Full text
Abstract:
A total of 65 skulls of the Australian sealion, Neophoca cinerea, was examined to investigate the extent to which sexual dimorphism is reflected in cranial dimensions (n = 32) and skull growth, and to determine whether cranial sutures (n = 18) can be useful in age determination. All adult skull dimensions studied display significant sexual dimorphism. Skull growth ceases close to 4–7 years of age for females (Suture Fusion Rating, SFR 25–34) but skull growth in males continues until at least 16 years of age. In animals with a SFR ≥� 25, male skulls have a minimum condylobasal length of 272 mm,
APA, Harvard, Vancouver, ISO, and other styles
2

Siismets, Erica M., and Nan E. Hatch. "Cranial Neural Crest Cells and Their Role in the Pathogenesis of Craniofacial Anomalies and Coronal Craniosynostosis." Journal of Developmental Biology 8, no. 3 (2020): 18. http://dx.doi.org/10.3390/jdb8030018.

Full text
Abstract:
Craniofacial anomalies are among the most common of birth defects. The pathogenesis of craniofacial anomalies frequently involves defects in the migration, proliferation, and fate of neural crest cells destined for the craniofacial skeleton. Genetic mutations causing deficient cranial neural crest migration and proliferation can result in Treacher Collins syndrome, Pierre Robin sequence, and cleft palate. Defects in post-migratory neural crest cells can result in pre- or post-ossification defects in the developing craniofacial skeleton and craniosynostosis (premature fusion of cranial bones/cr
APA, Harvard, Vancouver, ISO, and other styles
3

Wey, Philip D., Julie A. Neidich, Lloyd A. Hoffman, and Gregory S. Latrenta. "Midline Defects of the Orofaciodigital Syndrome Type VI (Váradi Syndrome)." Cleft Palate-Craniofacial Journal 31, no. 5 (1994): 397–400. http://dx.doi.org/10.1597/1545-1569_1994_031_0397_mdotos_2.3.co_2.

Full text
Abstract:
The orofaciodigital syndromes (OFDS) represent a spectrum of anomalies of the palate, cranium, hands, and feet. Váradi syndrome, designated OFDS type VI, is a rare disorder that is additionally characterized by cerebellar anomalies. The following report is of a patient with OFDS VI and characteristic multiple midline defects: median cleft lip and palate, lingual cleft with nodules, and midline brain malformation. In addition, this case is uniquely associated with the presence of midline (metopic and sagittal) craniosynostoses as well. It is unusual that deformities which result from premature
APA, Harvard, Vancouver, ISO, and other styles
4

Taniyama, Tomohide, Noriyuki Kitai, Yoshitaka Iguchi, Shumei Murakami, Miho Yanagi, and Kenji Takada. "Craniofacial Morphology in a Patient with Simpson-Golabi-Behmel Syndrome." Cleft Palate-Craniofacial Journal 40, no. 5 (2003): 550–55. http://dx.doi.org/10.1597/1545-1569_2003_040_0550_cmiapw_2.0.co_2.

Full text
Abstract:
Objective We present the case of a 6-year-old boy with a coarse face, cleft palate, and malocclusion with anterior open bite who had been diagnosed with Simpson-Golabi-Behmel syndrome. Morphology of the craniofacial structures was examined on the basis of conventional radiographs, three-dimensional (3D) computed tomography (CT) and magnetic resonance (MR) scanning. Patient This patient had 13 ribs on the right side, slight scoliosis, supernumerary nipples, a coarse face, hypertelorism, a short broad upturned nose, a wide mouth, a straight facial profile with incompetence of the lips, midline g
APA, Harvard, Vancouver, ISO, and other styles
5

Mooney, Mark P., H. Wolfgang Losken, Michael I. Siegel, et al. "Development of a Strain of Rabbits with Congenital Simple Nonsyndromic Coronal Suture Synostosis Part II: Somatic and Craniofacial Growth Patterns." Cleft Palate-Craniofacial Journal 31, no. 1 (1994): 8–16. http://dx.doi.org/10.1597/1545-1569_1994_031_0008_doasor_2.3.co_2.

Full text
Abstract:
In the March 1993 issue of The Cleft Palate-Craniofacial Journal we reported a female rabbit born in our laboratory with complete bilateral coronal suture (CS) synostosis. This follow-up study presents our attempts to breed the animal and establish a strain of craniosynostotic rabbits. The second part of this study presents longitudinal somatic and craniofacial growth data in offspring with coronal suture synostosis. Serial growth data from 72 animals were collected for the present study. The sample consisted of 11 animals (10 offspring and the original female) with complete nonsyndromic unila
APA, Harvard, Vancouver, ISO, and other styles
6

Siebert, Joseph R., Bryan Williams, Darin Collins, Linda A. Winkler, and Daris R. Swindler. "Spontaneous Cleft Palate in a Newborn Gorilla (Gorilla gorilla gorilla)." Cleft Palate-Craniofacial Journal 35, no. 5 (1998): 436–41. http://dx.doi.org/10.1597/1545-1569_1998_035_0436_scpian_2.3.co_2.

Full text
Abstract:
Objective We report the first case of cleft palate in a newborn male gorilla (Gorilla gorilla gorilla). Case History and Results The full-term infant was born to clinically healthy, wild-caught parents and survived 5 days. Autopsy disclosed a unilateral cleft palate, moderate scalp hemorrhage (birth versus postnatal trauma), cerebral edema, and a sterile fibrin vegetation in the heart. The palate was also shorter and narrower than expected, and the biorbital breadth was reduced; otherwise, growth and development appeared normal. Standard cranial and intraoral radiographs and three-dimensional
APA, Harvard, Vancouver, ISO, and other styles
7

Reddy, K. Venkataramana, Chapay Soren, M. Geethika, and V. Malathi. "Two cases with pycnodysostosis in a family: a case report." International Journal of Contemporary Pediatrics 7, no. 6 (2020): 1441. http://dx.doi.org/10.18203/2349-3291.ijcp20202164.

Full text
Abstract:
Pycnodysostosis (Greek, pycnos - density, dys - defect, ostosis - bone) is a rare inherited disorder of the bone, first described by Maroteaux and Lamy. Pycnodysostosis is an autosomal recessive disorder, with incidence estimated to be 1.7 per 1 million births. Clinical presentation of this disorder include short stature, dolichocephalic skull, frontal bossing, obtuse mandibular angle, dysplastic clavicles, and short hands and feet, diffuse osteosclerosis, acro-osteolysis along with the finger and nail abnormalities. The main oral aspects are midfacial hypoplasia, a grooved palate, and dental
APA, Harvard, Vancouver, ISO, and other styles
8

Khmara, T. V., M. O. Ryznychuk, N. B. Kuzniak, S. P. Melnychuk, S. O. Batranovska, and I. I. Zamorskii. "Ontology of Variants of the Structure and Malformations of the Skull. Part II. Hereditary Syndromes." Ukraïnsʹkij žurnal medicini, bìologìï ta sportu 6, no. 3 (2021): 71–77. http://dx.doi.org/10.26693/jmbs06.03.071.

Full text
Abstract:
Congenital abnormalities occur in 2-3% of all children and about 1% have hereditary syndromes or multiple malformations. About 30% of all cases have a cleft lip or palate. Genetic factors such as chromosomal abnormalities and gene mutations cause about 15% of congenital abnormalities; exogenous environmental factors cause about 10% of defects; a combination of genetic and environmental factors (multifactorial inheritance) cause 20-25%; multiple pregnancy causes 0.5-1% of congenital abnormalities. Craniofacial anomalies represent an important pediatric problem. They are among the leading causes
APA, Harvard, Vancouver, ISO, and other styles
9

Khmara, T. V., N. B. Kuzniak, Y. A. Morarash, M. O. Ryznychuk, A. Ye Petriuk, and M. P. Kavun. "Ontology of Variants of Cranial Structure and Malformations. Part I." Ukraïnsʹkij žurnal medicini, bìologìï ta sportu 6, no. 2 (2021): 20–30. http://dx.doi.org/10.26693/jmbs06.02.020.

Full text
Abstract:
Annually severe congenital abnormalities occur in 1 of 33 newborns or about 125.000 live births in the United States and are the leading cause of infant mortality. Craniofacial anomalies account for about one-third of all abnormalities. The prevalence of human congenital malformations is an important characteristic of public health. According to the World Health Organization, the birth rate of children with cleft lip and palate is on average 1:750 newborns, which is 20-30% of all human malformations and 86% of maxillofacial malformations. They contribute significantly to infant morbidity and d
APA, Harvard, Vancouver, ISO, and other styles
10

Leahey, Lucy G., Ralph E. Molnar, Kenneth Carpenter, Lawrence M. Witmer, and Steven W. Salisbury. "Cranial osteology of the ankylosaurian dinosaur formerly known asMinmisp. (Ornithischia: Thyreophora) from the Lower Cretaceous Allaru Mudstone of Richmond, Queensland, Australia." PeerJ 3 (December 8, 2015): e1475. http://dx.doi.org/10.7717/peerj.1475.

Full text
Abstract:
Minmiis the only known genus of ankylosaurian dinosaur from Australia. Seven specimens are known, all from the Lower Cretaceous of Queensland. Only two of these have been described in any detail: the holotype specimenMinmi paravertebrafrom the Bungil Formation near Roma, and a near complete skeleton from the Allaru Mudstone on Marathon Station near Richmond, preliminarily referred to a possible new species ofMinmi. The Marathon specimen represents one of the world’s most complete ankylosaurian skeletons and the best-preserved dinosaurian fossil from eastern Gondwana. Moreover, among ankylosaur
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Palate Cranial sutures"

1

Beauthier, Jean-Pol. "Contribution à l'approche anthropologique et médico-légale des sutures viscérocrâniennes utiles dans l'estimation de l'âge au décès (Sutures palatines, fronto-naso-maxillaires et zygomatiques)." Doctoral thesis, Universite Libre de Bruxelles, 2009. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/210228.

Full text
Abstract:
Les sutures crâniennes ont été régulièrement étudiées au fil des siècles puisque déjà Vésale établissait une relation entre l’âge et la synostose suturale.<p><p>Leur imprécision a quelque peu confiné l’observation de ces sutures dans un certain oubli, justifié en partie.<p><p>Il est clair que leur fiabilité quant à l’estimation de l’âge au décès reste discutable et ce, pour diverses raisons.<p><p>Leur observation est difficile et dès lors sujette à subjectivité dans l’appréciation de leurs stades de fusion.<p><p>De plus, leur apparence sur le crâne sec peut être altérée par divers artéfacts de
APA, Harvard, Vancouver, ISO, and other styles
2

Cerrone, Junior Giovanni. "Avaliação da densidade mineral das suturas palatina mediana e zigomaticomaxilar em diferentes faixas etárias por tomografia computadorizada de feixe cônico." Universidade Federal de Juiz de Fora (UFJF), 2010. https://repositorio.ufjf.br/jspui/handle/ufjf/2720.

Full text
Abstract:
Submitted by Renata Lopes (renatasil82@gmail.com) on 2016-10-04T19:49:28Z No. of bitstreams: 1 giovannicerronejunior.pdf: 817886 bytes, checksum: 0fa932ad0501da4870ddd992b78ab4e1 (MD5)<br>Approved for entry into archive by Diamantino Mayra (mayra.diamantino@ufjf.edu.br) on 2016-10-05T10:52:53Z (GMT) No. of bitstreams: 1 giovannicerronejunior.pdf: 817886 bytes, checksum: 0fa932ad0501da4870ddd992b78ab4e1 (MD5)<br>Made available in DSpace on 2016-10-05T10:52:53Z (GMT). No. of bitstreams: 1 giovannicerronejunior.pdf: 817886 bytes, checksum: 0fa932ad0501da4870ddd992b78ab4e1 (MD5) Previous is
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Palate Cranial sutures"

1

Hefner, Joseph T., and Kandus C. Linde. "Transverse Palatine Suture." In Atlas of Human Cranial Macromorphoscopic Traits. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-12-814385-8.00018-5.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Palate Cranial sutures' for particular source types:
Journal articles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography