Publications by authors named "Hagit Sadis"

Article Synopsis
  • - Smith-Magenis Syndrome (SMS) is a rare genetic disorder linked to intellectual disability, behavioral issues, and sleep problems, caused by a deletion in the chromosome band 17p11.2 affecting the RAI1 gene.
  • - RAI1 plays a role in neurodevelopment and may be connected to Parkinson's disease (PD), which is characterized by motor symptoms like tremors and bradykinesia.
  • - A case study of a patient with both SMS and early-onset PD raises questions about the relationship between RAI1 gene variations and PD, highlighting the need for more research and attention from caregivers regarding potential PD symptoms in SMS patients.
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Schizophrenia affects approximately 1% of the world population. Genetics, epigenetics, and environmental factors are known to play a role in this psychiatric disorder. While there is a high concordance in monozygotic twins, about half of twin pairs are discordant for schizophrenia.

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