Holoprosencephaly with Multiple Anomalies of the Craniofacial Bones-An Autopsy Report

Holoprosencephaly with multiple anomalies of the craniofacial bones-an autopsy report.

Holoprosencephaly (HPE), a disorder which results from a failure of cleavage or the incomplete differentiation of the forebrain structures at various levels or to various degrees, is related to hereditary factors, chromosomal anomalies, cytogenetic abnormalities, and environmental teratogenic factors. We are reporting a case of a multiparous woman who was G3,P3,L2, who delivered a full term foe...

Septopreoptic holoprosencephaly: a mild subtype associated with midline craniofacial anomalies.

SUMMARY HPE is a congenital brain malformation characterized by failure of the prosencephalon to divide into 2 hemispheres. We have identified 7 patients who have a mild subtype of HPE in which the midline fusion was restricted to the septal region or preoptic region of the telencephalon. This subtype, which we call septopreoptic HPE, falls in the spectrum of lobar HPE, but lacks significant fr...

Global registry and database on craniofacial anomalies Report of a WHO Registry Meeting on Craniofacial Anomalies

an investigation of the types of text reduction in subtitling: a case study of the persian film gilaneh with english subtitles

چکیده ندارد.

Giant Cell Lesions of the Craniofacial Bones

Multinucleate giant cells of one type or another are commonly encountered in oral and maxillofacial lesions. These include the common occurrence of foreign-body-type giant cells in some reactive lesions, and giant cells associated with granulomatous inflammation as a consequence of infection. However in these cases the giant cells do not represent the primary pathology. In this brief review, we...