RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164071430
T1 Gorlin-Chaudhry-Moss 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=1164071430
RD 2024/04/23
AB A  very  rare  syndrome  characterized  by  craniosynostosis,  midfacial  hypoplasia,  hypertrichosis,  and  anomalies  of  the  heart  (stenosis  of  the  aortic  and  pulmonary  valves),  eyes,  teeth,  and  external  genitalia.  Mental  retardation  has  been  observed.