Finding a diagnosis: Diseases that mimic TK2d symptoms
Making sure your care team is aware of both TK2d and its differential diagnoses is key to proper care.
Making sure your care team is aware of both TK2d and its differential diagnoses is key to proper care.
It is helpful to recognize the real benefits to health and wellbeing, not just the losses.
A muscle biopsy measures the levels of mitochondrial DNA depletion and also serves to clarify certain aspects of the disease.
Many patients with TK2d are eventually unable to speak clearly enough to be understood by others.
Landmarks worldwide will light up on Rare Disease Day.
In infants with TK2d, encephalopathy can mean seizures, cognitive difficulties and impaired hearing.
Early diagnosis means early treatment and the chance to slow down the disease.
A physical therapist can help maintain muscle function and range of motion as TK2d progresses.
A feeding tube means patients with TK2d can get nutrients without the risk of choking.
Recruitment company Rare Patient Voice has more than 200,000 registered patients and family caregivers spanning rare, chronic and complex conditions.