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Results for “Maxillofacial Development”

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Differences in protocols of craniofacial development related to twinship and zygosity.

Using 56 adult dental diameters as a subsystem model for craniofacial development, we show that monozygotic (MZ), dizygotic (DZ), and singleton groups differ significantly in developmental relationships assessed by multivariate statistical methods under commonly accepted assumptions. Given the differences observed, we suggest that any assumption of developmental equivalence between MZ and DZ twins, or between twins of either group and singletons, for variables of craniofacial or behavioral development, may be subject to serious doubt. Implications for twin study theory and methodology, and for study of early human development, are discussed.

Birth Order↗

[The role of apoptosis during craniofacial development: concepts and importance in pathology].

Apoptosis is an essential common final pathway in numerous pathological conditions such as malignant tumors, HIV-related CD4 lymphocytes degeneration, neurodegenerative disorders, and in programmed cell death events during normal embryogenesis. Some teratogenic substances for man and laboratory mammals induce an increase of the apoptotic phenomenon, responsible for the occurrence of some precise cranio-maxillo-facial malformations. The study of cell death during normal or teratogenic embryonic development allows to analyse the cellular mechanisms implied in the control of the apoptotic phenomenon, together with its dysregulation ending in pathological processes. We review the cell death phenomenon during cephalogenesis, both during normal embryogenesis, or in teratogenic conditions known to induce cranio-maxillo-facial malformations.

Abnormalities, Drug-Induced↗