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Reaching Out The Newsletter of the Cornelia de Lange Syndrome (CdLS) USA Foundation, Inc.Second Quarter 2017Highlights Directors Message: The Yellow Brick Road to AwarenessSpotlights: Sleep and CdLS
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Cornelia de Lange Syndrome is a genetic disorder affecting numerous aspects of a person's physical and cognitive development. The syndrome primarily affects infants and children, but individuals of all ages who have Cornelia de Lange Syndrome may require care, support, and specialized services. The following individuals or groups may need Cornelia de Lange Syndrome:
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Cornelia de Lange syndrome (CdLS) is a rare genetic disorder that affects physical, cognitive, and developmental health, characterized by distinct facial features, limb abnormalities, and various health issues.
There are no specific filing requirements for individuals with Cornelia de Lange syndrome; rather, it is a medical diagnosis. However, medical professionals and researchers may need to report cases for statistical and treatment purposes.
Since Cornelia de Lange syndrome is a medical condition rather than a form or document, there is no 'filling out' process. Diagnosis and management are done through medical assessments and evaluations.
The purpose of identifying Cornelia de Lange syndrome is to provide appropriate medical care, support, and resources for affected individuals and their families, along with increasing awareness and understanding of the condition.
Information regarding clinical characteristics, genetic findings, treatment plans, and patient demographics may be reported in medical settings to aid in research and improve care for individuals with CdLS.
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