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, 2010]. In addition, other malformations may be found such as underdeveloped mammae, urinary tract defects, facial cleft, cleft lip and palate, caudal tails and anal malpositioning. Intellectual functioning is usually normal or mildly delayed. Variation of expressivity is evident. Mutations in the X-linked PORCN gene can be identified in all patients with a classical Goltz�CGorlin phenotype [Maas et al., 2009]. No obvious genotype-phenotype correlation has been observed to date [Lombardi et al., submitted for publication]. The pentalogy of Cantrell (Cantrell�CHaller�CRavitsch syndrome) is a rare, severe and usually lethal congenital disorder, the incidence Selleckchem Metformin being estimated at 1 in 65,000 live births. The condition is characterized by the combination of five anomalies: a midline supra-umbilical abdominal wall defect (i.e., omphalocele, gastroschisis, absent umbilicus, diastasis of the recti); defect of lower sternum (i.e., absent or cleft sternum); deficiency of the diaphragmatic selleckchem pericardium (ectopia cordis, free communication between pericardial and peritoneal cavities), deficiency of the anterior diaphragm (i.e., anterior diaphragmatic hernia, hypoplastic diaphragm); and congenital heart anomalies (i.e., ASD, VSD, AS, Fallot tetralogy, double outlet right ventricle, truncus arteriosus, anomalous pulmonary venous drainage, left ventricular diverticulum, hypoplastic left heart, Alkannin tricuspid atresia). Cantrell pentalogy is often incompletely present: the full pentalogy is diagnosed rarely, as various combinations of two or three of four defects of the pentalogy are more common [Cantrell et al., 1958; Toyama, 1972; van Allen et al., 1987; Vanamo et al., 1991; Carmi and Boughman, 1992; Fernandez et al., 1997; Polat et al., 2005; van Hoorn et al., 2008]. We describe a female infant with severe developmental abnormalities resembling Cantrell pentalogy as well as distinctive facial and limb manifestations, clinically diagnosed as Goltz�CGorlin syndrome. Molecular analysis revealed a sporadic point mutation in PORCN. We review the existing literature describing patients with phenotypes that show an overlap with the two entities. The proposita was born by cesarean delivery because of suspicion of omphalocele at 38 weeks of gestation to a 29-year-old G2P1 mother and a 32-year-old father. Routine fetal ultrasound at 22nd week of gestation had shown intrauterine growth retardation and suggested cleft hands. The remainder of the fetal anatomy appeared normal at that time. At birth she weighted 2060?g (