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 2024/04/18
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.