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1Tuberous Sclerosis Complex: Measuring Parental Stress, Depression and Quality of Life. Khayelihle Chagadama (CHGKHA003) ABSENT Laboratory Supervisor: Dr. Susan Malcolm Smith Supervisor: Tenable PageDepartment
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Tuberous sclerosis complex is a rare genetic disorder that can affect anyone. It is typically diagnosed in early childhood or infancy. Individuals who exhibit symptoms such as seizures, developmental delays, and skin abnormalities may need to be evaluated for tuberous sclerosis complex. Additionally, individuals with a family history of the condition may also need to be screened for this disorder.
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Tuberous sclerosis complex is a rare genetic disorder that causes noncancerous (benign) tumors to grow in the brain and other vital organs.
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The reporting of tuberous sclerosis complex typically involves filling out a standardized form with information about the patient's medical history and diagnostic findings.
The purpose of reporting tuberous sclerosis complex is to track the incidence and prevalence of the disorder, as well as to facilitate research and improve patient care.
Information such as patient demographics, symptoms, diagnostic tests, treatment plans, and outcomes must be reported on tuberous sclerosis complex.
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