Autopsy and Case Reports
Autopsy and Case Reports
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Alobar holoprosencephaly and Trisomy 13 Patau syndrome

Andressa Dias Costa; Regina Schultz; Sérgio Rosemberg

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Holoprosencephaly (HPE) is a congenital defect of the brain, median structures, and face resulting from an incomplete cleavage of the primitive brain during early embryogenesis. The authors report a case of trisomy 13 syndrome diagnosed at prenatal follow up. The preterm newborn lived only 5 hours, and died because of severe respiratory failure. The autopsy findings disclosed facial, skull, limbs, cardiac, and cerebral malformations. Among the latter, the presence of alobar HPE, the central theme of this report, was evident. The most common nonrandom chromosomal abnormality in patients with HPE is trisomy 13. The most severe variant, namely alobar HPE, is shown in this case report. Discussion on this severe anomaly, along with the case report with details of Patau’s syndrome, is the goal of this report.


Holoprosencephaly, Nervous System Malformations, Patau syndrome, Autopsy.

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569696a564cc8b5cda711bc1 autopsy Articles
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