Tetralogy of Fallot

Tetralogy of Fallot is a congenital cardiac malformation that consists of an interventricular communication, also known as a ventricular septal defect, obstruction of the right ventricular outflow tract, override of the ventricular septum by the aortic root, and right ventricular hypertrophy.

Prominent forehead

Forward prominence of the entire forehead, due to protrusion of the frontal bone.


Total: 2

                       


(per page)
PMID (PMCID)
18536049
 FEMALE Infant
Delineation of the proximal 3q microdeletion syndrome.
Simovich MJ, Bland SD, Peiffer DA, Gunderson KL, Cheung SW, Yatsenko SA, Shinawi M.
Am J Med Genet A. 2008;146A(13):1729-35.
The patient has distinct facial features including brachycephaly, broad and prominent forehead, flat nasal bridge, prominent ears, anteverted nose, tetralogy of Fallot, bilateral cryptorchidism, and peripheral skeletal abnormalities.
17041938
 FEMALE Infant, Newborn
Frontonasal malformation, first branchial arch anomalies, congenital heart defect, and severe central nervous system involvement: a possible "new" autosomal recessive syndrome?
Guion-Almeida ML, Richieri-Costa A.
Am J Med Genet A. 2006;140(22):2478-81.
Here we report on a girl presenting with midline cleft lip/palate, prominent forehead, macrocephaly, first branchial arch anomalies, and tetralogy of Fallot.