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16p11.2 deletion syndrome is considered to have an autosomal dominant inheritance pattern because a deletion in one copy of chromosome 16 in each cell is sufficient to cause the condition. Author information: (1)Institute of Human Genetics, Technische Universität München, Munich, Germany. We report on a further patient with a microdeletion 16p11.2‐p12.2 in the context of described patients with a deletion in the pericentromeric region of 16p. Hempel M(1), Rivera Brugués N, Wagenstaller J, Lederer G, Weitensteiner A, Seidel H, Meitinger T, Strom TM. 16p11.2 deletion syndrome is mainly characterized by some degree of … 16p11.2 Deletion Syndrome is a condition caused by a missing piece (deletion) on a specific region of chromosome 16 designated as p11.2 People with 16p11.2 Deletion Syndrome usually have developmental delay and intellectual disability. Minor facial anomalies, feeding difficulties, significant delay in speech development, and recurrent ear infections are common symptoms of the microdeletion syndrome 16p11.2‐p12.2. However, most cases of 16p11.2 deletion syndrome are not inherited.The deletion occurs most often as a random event during the formation of reproductive cells (eggs and sperm) or in early fetal … Microdeletion syndrome 16p11.2-p12.2: clinical and molecular characterization.