RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164070647 T1 Genoa Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164070647 RD 2024/10/08 AB Extremely rare syndrome with primary craniosynostosis and holoprosencephaly (HPE). Newborn with this condition show failure of the developing brain to sufficiently divide into two separate cerebral hemispheres. This medical condition is part of a group of semilobar HPE. Endocrinopathies are associated with HPE and consist of diabetes insipidus (DI), hypothyroidism, hypocortisolism, and growth hormone deficiency.