Literature DB >> 17101024

Fetal alcohol syndrome and developing craniofacial and dental structures--a review.

L B Sant'Anna1, D O Tosello.   

Abstract

OBJECTIVES: Fetal alcohol syndrome (FAS) is a collection of signs and symptoms seen in children exposed to alcohol in the prenatal period. It is characterized mainly by a distinct pattern of craniofacial malformations, physical and mental retardation. However, with the increased incidence of FAS, there is a great variation in the clinical features of FAS.
DESIGN: Narrative review.
RESULTS: This review describes data from clinical and experimental studies, and in vitro models. Experimental studies have shown that alcohol has a direct toxic effect on the ectodermal and mesodermal cells of the developing embryo, particularly in the cells destined to give rise to dentofacial structures (i.e. cranial neural crest cells). Other effects, such as, abnormal pattern of cranial and mandibular growth and altered odontogenesis are described in detail. The exact mechanism by which alcohol induces its teratogenic effects remains still unknown. The possible mechanisms are outlined here, with an emphasis on the developing face and tooth. Possible future research directions and treatment strategies are also discussed.
CONCLUSION: Early identification of children affected by prenatal alcohol exposure leads to interventions, services, and improved outcomes. FAS can be prevented with the elimination of alcohol consumption during pregnancy. We need to provide education, target high-risk groups, and make this issue a high priority in terms of public health.

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Year:  2006        PMID: 17101024     DOI: 10.1111/j.1601-6343.2006.00377.x

Source DB:  PubMed          Journal:  Orthod Craniofac Res        ISSN: 1601-6335            Impact factor:   1.826


  16 in total

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2.  Vasoactive exposures during pregnancy and risk of microtia.

Authors:  Carla M Van Bennekom; Allen A Mitchell; Cynthia A Moore; Martha M Werler
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2012-11-24

Review 3.  Suckling, Feeding, and Swallowing: Behaviors, Circuits, and Targets for Neurodevelopmental Pathology.

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4.  Lobeline attenuates neonatal ethanol-mediated changes in hyperactivity and dopamine transporter function in the prefrontal cortex in rats.

Authors:  A M Smith; K A Wellmann; T M Lundblad; M L Carter; S Barron; L P Dwoskin
Journal:  Neuroscience       Date:  2011-11-20       Impact factor: 3.590

5.  Neurofibromatosis Type 1 With Cherubism-like Phenotype, Multiple Osteolytic Bone Lesions of Lower Extremities, and Alagille-syndrome: Case Report With Literature Survey.

Authors:  Reinhard E Friedrich; Jozef Zustin; Andreas M Luebke; Thorsten Rosenbaum; Martin Gosau; Christian Hagel; Felix K Kohlrusch; Ilse Wieland; Martin Zenker
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6.  Normalized shape and location of perturbed craniofacial structures in the Xenopus tadpole reveal an innate ability to achieve correct morphology.

Authors:  Laura N Vandenberg; Dany S Adams; Michael Levin
Journal:  Dev Dyn       Date:  2012-03-23       Impact factor: 3.780

7.  Phenotypic diversity in white adults with moderate to severe Class II malocclusion.

Authors:  Lina M Moreno Uribe; Sara C Howe; Colleen Kummet; Kaci C Vela; Deborah V Dawson; Thomas E Southard
Journal:  Am J Orthod Dentofacial Orthop       Date:  2014-03       Impact factor: 2.650

8.  Beliefs about fetal alcohol spectrum disorder among men and women at alcohol serving establishments in South Africa.

Authors:  Lisa A Eaton; Eileen V Pitpitan; Seth C Kalichman; Kathleen J Sikkema; Donald Skinner; Melissa H Watt; Desiree Pieterse; Demetria N Cain
Journal:  Am J Drug Alcohol Abuse       Date:  2014-03       Impact factor: 3.829

Review 9.  The Genetics of Fetal Alcohol Spectrum Disorders.

Authors:  Johann K Eberhart; Scott E Parnell
Journal:  Alcohol Clin Exp Res       Date:  2016-04-28       Impact factor: 3.455

10.  Ethanol disrupts chondrification of the neurocranial cartilages in medaka embryos without affecting aldehyde dehydrogenase 1A2 (Aldh1A2) promoter methylation.

Authors:  Yuhui Hu; Kristine L Willett; Ikhlas A Khan; Brian E Scheffler; Asok K Dasmahapatra
Journal:  Comp Biochem Physiol C Toxicol Pharmacol       Date:  2009-08-03       Impact factor: 3.228

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