TY  - CHAP
M1  - Book, Section
TI  - Common Dysmorphic Syndromes
A1  - Zadeh, Neda
A2  - Stevenson, David K.
A2  - Cohen, Ronald S.
A2  - Sunshine, Philip
Y1  - 2015
N1  - 
T2  - Neonatology: Clinical Practice and Procedures
AB  - Numerous  genetic  conditions  are  evident  and  diagnosable  during  the  neonatal  period  because  of  a  specific  pattern  of  clinical  features  often  present  on  infant  physical  examination.  This  chapter  reviews  several  of  the  more  frequently  observed  genetic  dysmorphic  conditions  neonatal  practitioners  are  most  likely  to  encounter  in  a  newborn  (apart  from  the  common  trisomies  that  are  addressed  separately  in  this  textbook),  which  include:  Turner  syndrome  (TS),  22q11.2  deletion  syndrome,  CHARGE  (coloboma,  heart  defect,  atresia  choanae  [also  known  as  choanal  atresia],  retarded  growth  and  development,  genital  abnormality,  and  ear  abnormality)  syndrome,  and  VACTERL  (vertebral,  anal,  cardiac,  tracheoesophageal,  renal,  and  limb)  association.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/19
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1109799442
ER  -