TY  - CHAP
M1  - Book, Section
TI  - Holt-Oram Syndrome (HOS)
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
Y1  - 2019
N1  - 
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - Genetically  transmitted  malformation  syndrome  characterized  by  congenital  anomalies  of  the  upper  extremity  malformations  involving  radial,  thenar  (hypoplasia  or  triphalangeal  thumb),  or  carpal  bones  associated  with  heart  disease  (ventricular  and  atrial  septal  defect  as  well  as  conduction  problems).  This  medical  condition  can  also  affect  other  part  of  the  skeletal  structure.  It  is  reported  that  approximately  75%  of  individuals  with  Holt-Oram  Syndrome  have  severe  heart  problems.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/19
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164073080
ER  -