Estivill X. Physical and occupational therapy may be beneficial, depending on the specific motor impairments. Goto, M.
Am J Med Genet A. Somatic and germ-line mosaicism of deletion 15q Adults with Angelman syndrome have distinctive facial features that may be described as "coarse.
Medications used for minor motor seizures e. An unexpected recurrence of Angelman syndrome suggestive of maternal germ-line mosaicism of del 15 q11q13 in a Finnish family. Prenat Diagn. The second is a fairly specific laughing response, induced by striking a tuning fork that is held out of sight but within hearing range of the child with Angelman syndrome.
Other children may have a genetic syndrome that looks like AS but is caused by a different gene. Clinical, cytogenetical and molecular analyses of Angelman syndrome. The disorder results from the absence of the UBE3A gene inherited from the mother.
Angelman syndrome in Denmark. Primary cell cultures from fetal mouse brain have demonstrated that UBE3A imprinting is limited to neurons, but glial cells show biallelic expression [ Yamasaki et al ]. Ophthalmic findings in Angelman syndrome.