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2 Possible Causes for 10% due to Paternal Deletion

  • Frasier Syndrome

    paternally expressed genes, either due to deletion of region, maternal UPD, accidental paternal imprinting disease characterized by mental retardation, microcephaly, macrosomia[] […] structures and all male has placenta, no fetus disease characterized by neonatal hypotonia, hyperphagia, obesity, short stature, hypopigmentation; caused by loss of function of 10[]

  • Prader-Willi Syndrome

    The majority of cases of PWS (70–75%) are due to deletions on the paternally inherited chromosome 15 ( 9 ), with the remainder caused mainly by maternal uniparental disomy[] […] for region 15q11–13 ( 10 ).[]

Further symptoms