RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164086777
T1 Trisomy 4p
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=1164086777
RD 2024/04/24
AB A  rare  chromosomal  disorder  in  which  all  or  a  portion  of  the  short  arm  (p)  appears  three  times  rather  than  twice  in  cells  of  the  body.  It  is  clinically  characterized  by  breathing  difficulties,  craniofacial  anomalies,  hands  and  feet  abnormalities,  and  congenital  heart  defects.  Other  clinical  features  include  genital  anomalies  in  affected  males,  skeletal  defects,  and  severe  mental  retardation.