RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164077652
T1 Malpuech 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=1164077652
RD 2024/04/25
AB It  is  a  genetic  disorder  characterized  by  an  association  of  mental  retardation,  dwarfism,  hypertelorism,  facial  clefting  (lip  and  palate),  and  caudal  appendage.  Other  features  include  urogenital  abnormalities  (micropenis,  hypospadias,  renal  anomalies),  malar  hypoplasia,  large  fontanelle,  omphalocele,  seizures,  polycystic  kidneys,  and  deafness.  Cardiac  and  renal  abnormalities  may  also  be  present.