RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164081352
T1 Penta X 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=1164081352
RD 2024/04/17
AB A  rare  chromosomal  disorder  manifested  by  the  presence  of  five  X  chromosomes  leading  to  short  stature,  mental  retardation,  fifth  finger  clinodactyly,  short  neck,  microcephaly,  cardiac  anomalies  (ventricular  septal  defect,  atrial  septal  defect,  patent  ductus  arteriosus),  and  horseshoe  kidneys.  Onset  is  during  childhood.