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Turner Syndrome and Special Education Provisions in mainstream Irish Primary Schools. Linda Falconer dissertation submitted in part fulfillment of the requirement for the B.A.(hons) Degree in Health Promotion
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Turner syndrome is a genetic disorder that only affects females. It occurs when one of the two X chromosomes is partially or completely missing. Therefore, individuals who have been diagnosed or suspected to have Turner syndrome would need specialized care and management.
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Specialists who work with individuals with Turner syndrome include geneticists, endocrinologists, cardiologists, gynecologists, and other healthcare professionals familiar with the condition. They provide comprehensive care and support to help manage the medical, physical, and emotional aspects associated with Turner syndrome.
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Turner syndrome is a genetic condition that affects females and is caused by a missing or incomplete X chromosome. Individuals with Turner syndrome may have a variety of physical and developmental characteristics and may require special health care or educational support.
Individuals diagnosed with Turner syndrome and those who provide care or support for them may need to file relevant documentation or applications related to health care, educational services, or disability benefits.
To fill out documents related to Turner syndrome, one typically needs to provide personal information, medical history, and any special accommodations or support required. It is advisable to follow the specific forms and guidelines set by the relevant authority.
The purpose of documents related to Turner syndrome is to ensure that affected individuals receive the necessary support, services, and accommodations they require for their health, education, and overall well-being.
Information that may need to be reported includes the individual's diagnosis, medical history, specific needs or accommodations, and any other relevant data that supports the individual's eligibility for services or benefits.
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