Results 241 to 250 of about 34,364 (292)

Craniofacial developmental abnormalities

Current Opinion in Neurology, 1998
Major advances have been made in the elucidation of the molecular basis of a number of human dysmorphic syndromes involving abnormalities of craniofacial development. This will lead, in turn, to a greater understanding of the mechanisms that underlie normal craniofacial development.
F V, Elmslie, W, Reardon
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The airway in patients with craniofacial abnormalities

Paediatric Anaesthesia, 2004
SummaryAirway management for patients with craniofacial disorders poses many challenges. The anaesthesiologist must be familiar with the normal bony and soft‐tissue anatomy in the airway and how anatomy is altered by various congenital disorders. Specific areas to assess include the oral cavity, anterior mandibular space, maxilla, temporomandibular ...
exaly   +3 more sources

Abnormal craniofacial growth

Acta Odontologica Scandinavica, 1995
Treatment of patients with craniofacial (CF) anomalies necessitates knowledge about normal CF growth and how it deviates in the abnormal state. There are different basic types of CF anomalies and various kinds of aberrations that influence CF development. These factors might help to explain why patients display growth variations.
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Diagnostic approaches to respiratory abnormalities in craniofacial syndromes

Seminars in Fetal and Neonatal Medicine, 2021
Craniofacial syndromes are a complex cluster of genetic conditions characterized by embryonic perturbations in the developmental trajectory of the upper airway and related structures. The presence of reduced airway size and maladaptive neuromuscular responses, particularly during sleep, leads to significant alterations in sleep architecture and overall
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Abnormal Coagulation during Pediatric Craniofacial Surgery

Pediatric Neurosurgery, 2001
<i>Introduction:</i> This prospective study of children undergoing major craniofacial surgery was undertaken to determine whether abnormal hemostasis occurred and to characterize any coagulopathy found. <i>Methods:</i> Coagulation tests, blood loss and blood product transfusions were recorded perioperatively.
G D, Williams, R G, Ellenbogen, J S, Gruss   +2 more
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Abnormalities of craniofacial development: discussion report

Development, 1988
ABSTRACT The following topics arose as major areas of discussion after individual papers and in the general discussion at the end of the session. Discussion from both sources has been merged here to facilitate easier reading.
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The application of molecular genetics to detection of craniofacial abnormality

Development, 1988
ABSTRACT Congenital malformations such as secondary cleft palate can be exclusively monogenic or polygenic, but most cases have a multifactorial origin involving both environmental and genetic factors, making genetic analysis difficult.
G, Moore, A, Ivens, J, Chambers, A, Bjornsson, A, Arnason, O, Jensson, R, Williamson   +6 more
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Abnormal craniofacial development in cyclopic salmonid fishes

Journal of Morphology, 1992
AbstractDifferent types and degrees of “spontaneous” and artificially induced cyclopic malformation in fishes are defined. Symmetrical cyclopia ranges from approximation of the eyes, to partial merger of the eyes in the midline, to complete cyclopia with a single median eye.
Jessica A, Bolker, Keith S, Thomson
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Syndromes of Abnormal Craniofacial Contour

2001
Abstract Anencephaly is a congenital anomaly characterized by an open neural tube in the cephalic region with an exposed mass of degenerate neural tissue on the skull floor. The cranial vault is absent, producing characteristic bulging of the eyes and absence of the neck.
Robert J Gorlin, M Michael Cohen, Raoul C M Hennekam   +2 more
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Structural Abnormalities of the Craniofacial Complex and Congenital Malformations

Pediatric Clinics of North America, 1991
This article was meant to be a very cursory survey of the multiple defects that abnormal development can produce in all areas of the craniofacial complex. Careful examination for these abnormalities should lead the clinician to earlier referral of patients for additional examination by a genetics team.
A E, Poole, D A, Redford-Badwal
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