Also Known As
FPSFontaine progeroid syndromeGCM syndromeGCMSGorlin Chaudhry Moss syndromeGorlin-Chaudhry-Moss SyndromeGorlin-Chaudhry-Moss syndromePetty syndromePetty-Laxova-Wiedemann syndromecraniofacial dysostosis, hypertrichosis, Hypoplasia of labia majora, dental and eye anomalies, patent ductus arteriosus, and normal intelligencecraniofacial dysostosis, hypertrichosis, hypoplasia of labia majoracraniofacial dysostosis-genital, dental, cardiac anomalies syndromecranofacial dysostosis-hypertrichosis-hypoplasia of labia majora syndromedental and eye anomalies, patent ductus arteriosus, and normal intelligencedental and eye anomalies-patent ductus arteriosus-normal intelligence syndromeprogeroid syndrome Petty typeprogeroid syndrome congenital Petty typeprogeroid syndrome, Petty typeprogeroid syndrome, congenital, Petty typePetty Laxova Wiedemann syndromecraniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies
Definition
A rare premature aging syndrome characterized by pre-and postnatal growth retardation, a congenital premature-aged appearance with distinctive craniofacial dysmorphism (wide calvaria with large open anterior fontanel and wide metopic suture, broad forehead, small face, micrognathia), markedly diminished subcutaneous fat, cutis laxa and wrinkled skin, without delay in psychomotor development. Scant, brittle hair, hypoplastic nails and delayed, abnormal dentition, as well as hypoplastic distal phalanges, umbilical hernia and eye abnormalities (myopia/hyperopia, strabismus), are also commonly associated.