Understanding characteristics, conditions and treatment patterns among males diagnosed with Rett syndrome: an analysis of commercial health insurance claims
Author:
Affiliation:
1. Health Analytics, LLC, Columbia, MD 21045, USA
2. Senior Director, Health Economics & Outcomes Research, Acadia Pharmaceuticals, San Diego, CA 92130, USA
Abstract
Funder
ACADIA Pharmaceuticals
Publisher
Future Medicine Ltd
Subject
General Medicine
Link
https://www.futuremedicine.com/doi/pdf/10.2217/frd-2022-0023
Reference30 articles.
1. National Institute of Neurological Disorders and Stroke. Rett syndrome (2023). www.ninds.nih.gov/health-information/disorders/rett-syndrome
2. Genetic and Rare Diseases Information Center. Rett syndrome – about the disease (2023). https://rarediseases.info.nih.gov/diseases/5696/rett-syndrome
3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
4. Towards a better diagnosis and treatment of Rett syndrome: a model synaptic disorder
5. Parental origin of de novo MECP2 mutations in Rett syndrome
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1. Characteristics, conditions, and healthcare service utilization patterns of individuals diagnosed with Rett Syndrome: an analysis of administrative claims data;Future Rare Diseases;2023-09
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