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 - 2024/10/14 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1109799442 ER -