TY - CHAP M1 - Book, Section TI - Genoa Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/03 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164070647 ER -