RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164071536
T1 Granddad 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=1164071536
RD 2024/04/24
AB A  medical  condition  characterized  by  the  mnemonic  growth  retardation,  aged  facial  appearance,  normal  development,  decreased  subcutaneous  fat,  and  inherited  as  an  autosomal  dominant  inheritance.  The  clinical  presentation  is  associated  with  characteristic  facial  appearance  that  includes  triangular  facies,  prominent  forehead,  thin  or  absent  scalp  hair,  deep-set  eyes,  midfacial  hypoplasia,  prominent  nasal  septum  with  hypoplasia  of  the  alae  nasi,  prominent  ears,  and  thin  lips.