Hallervorden-Spatz disease is an inherited neurological disorder which causes issues with movement. It is a serious but a rare condition that worsens over time.
Hallervorden-Spatz Disease is a genetic disease which is caused by an inherited defect in the pantothenate kinase 2 (PANK2) gene. The PANK2 is a protein that controls the formation of coenzyme A and helps your body in converting fats, some amino acids, and carbohydrates into energy.
But in some cases, it is not caused by PANK2 mutation.
HSD is also known as neurodegeneration with brain iron accumulation. Some of the common symptoms include:
There is no cure for HSD so far. Treatment will vary from person to person and is done to relieve the symptoms. However, it may include both therapy and medication.
Physical therapy helps to reduce muscle rigidity, muscle spasms and other muscular issues.Speech therapy can be useful for dysphagia or speech impairment.
Methscopolamine bromide can be used for drooling. Baclofen can treat dystonia by providing relief to the muscles.Benztropine is an anticholingeric agent used to treat rigidity and tremors.Memantine, rivastigmine and donepezil may help in dementia.
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Read more articles on Hallervorden Spatz Disease Signs and Symptoms
Hallervorden-Spatz disease is a neurological disorder which is inherited. It has an effect on the movement and can worsen with time.read more
Treatment for Hallervorden Spatz Disease is symptomatic and supportive, and may include physical or occupational therapy, exercise physiology, and/or speech pathology.read more