Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case report

• Main Authors: D. Nistico' (Author), F. Guidolin (Author), C. O. Navarra (Author), M. Bobbo (Author), A. Magnolato (Author), A. P. D'Adamo (Author), E. Giorgio (Author), B. Pivetta (Author), E. Barbi (Author), P. Gasparini (Author), M. Cadenaro (Author), F. Sirchia (Author)
• Format: Book
• Published: BMC, 2020-05-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background Monosomy 1p36 is the most common terminal deletion syndrome with an autosomal dominant pattern of inheritance. This syndrome is defined by an extremely wide spectrum of characteristics; however, developmental delay and intellectual disability of various degree are present in all...