TY - CHAP M1 - Book, Section TI - Simpson-Golabi-Behmel Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - A rare X-linked recessive prenatal and postnatal overgrowth syndrome. Clinical features include abnormal sacrum, absent nails/claws, cleft palate most often associated with a cleft of the lower lip, coarse facial features, macroglossia, coloboma, congenital heart defects (ventricular septal defect, atrial septal defect), diaphragmatic hernia, hepatomegaly, fusion of cervical vertebra and limited extension, hydronephrosis, intestinal malrotation, kidney failure, macrocephaly, and increased risk of embryonal cancers. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164085264 ER -