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Molecular Mechanisms of Holoprosencephaly

✍ Scribed by Deeann E. Wallis; Maximilian Muenke

Book ID
115639579
Publisher
Elsevier Science
Year
1999
Tongue
English
Weight
187 KB
Volume
68
Category
Article
ISSN
1096-7192

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## Abstract Holoprosencephaly (HPE) has captivated the imagination of Man for millennia because its most extreme manifestation, the single‐eyed cyclopic newborn infant, brings to mind the fantastical creature Cyclops from Greek mythology. Attempting to understand this common malformation of the for

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Holoprosencephaly (HPE) is a common developmental anomaly of the forebrain and midface in which the cerebral hemispheres fail to separate into distinct left and right halves. HPE is extremely heterogeneous. In addition to teratogenic agents, several genes are implicated in the cause of HPE. Using sa

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## Abstract Holoprosencephaly is addressed under the following headings: alobar, semilobar, and lobar holoprosencephaly; arrhinencephaly; agenesis of the corpus callosum; pituitary abnormalities; hindbrain abnormalities; syntelencephaly; aprosencephaly/atelencephaly; neural tube defects; facial ano