Trattamenti di a malatia di Huntington à l'esteru
Huntington’s disease affects brain that worsens with time. There is no treatment that can reverse Huntington’s disease. Medicines and certain therapies help to manage the symptoms and supports the patient to adapt to the changes.
Huntington’s disease is a progressive brain disorder. In adults the disease usually appears in thirties or forties. The disease involves uncontrolled movement, mental and emotional problems, change in personality, etc.
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Therapies to manage Huntington’s disease
Following are the best 10 hospitals for Huntington's Disease Treatment in the world:
# | Hospital | paese | Certu | Prezzo | |
---|---|---|---|---|---|
1 | BLK-MAX Super Special Hospital | India | New Delhi | - - | |
2 | 'Uspitalu di Bangkok | Tailanda | Bangkok | - - | |
3 | Medipol Mega Ospedale Universitariu | Turchia | Istanbul | - - | |
4 | ISAR Klinikum Munich | Alemagna | Munich | - - | |
5 | Sun Medical Center | Corea di u Sudu | Daejeon | - - | |
6 | Ospedale Generale di Muro | Spagna | Mallorca | - - | |
7 | Ospedale Dar Al Fouad | Egittu | Cairo | - - | |
8 | CAMINÀ DI NOVE Centru | Alemagna | Berlin | - - | |
9 | Apollo Hospital Chennai | India | Chennai | - - | |
10 | Centru Medicu San Luca | Filippine | Città Quezon | - - |
Following are the best doctors for Huntington's Disease Treatment in the world:
# | DUTTORE | SPECIALITÀ | HOSPITALE |
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The cause of Huntington’s disease is an inherited defect in a gene.
• Involuntary movements • Emotional problems (depression, mood swings, etc) • Speech problem • Movement becomes slow • Memory loss and not able to focus • Cannot do multi tasks • Difficulty in swallowing • Loss of balance and coordination
The disease gets worse with the passing time. The disease becomes fatal after a period of almost 20 years.
Apart from history taking and physical examination, your doctor will recommend following diagnostic tools to rule out the disease – • Blood tests • Genetic testing • Imaging techniques such as MRI and CT scan
Huntington’s disease progresses over years. The 5 stages are – • Preclinical stage • Early stage • Middle stage • Late stage • End of life stage
One must have nutritious diet as the body may require high calories or there may be problem in metabolism. Your doctor will recommend the diet you must follow.
The disease usually appears in 30s and 40s. Rarely it may occur in children. In children the disease is called juvenile Huntington’s disease (JHD).
The main risk factor for Huntington’s disease is if the disease is in the family. Parents with HD have 50% chances the disease may develop in their children.
Huntington’s disease is a rare disease and its occurrence in children is even less.
Yes, Huntington’s disease is an inherited disease. Children with juvenile Huntington’s disease mostly inherit from their fathers.
Chorea is involuntary jerks and twisted movements. It is the first physical symptom in Huntington’s disease. It initially affects muscles of hands, fingers and face and later the extremities.
No, the disease cannot be prevented. Huntington’s disease occurs due to gene mutation and there is no way to stop the mutation.
Being a progressive brain disease, it important to ensure following things – • Eat a healthy and balanced food • Drink lot of water • Exercise in routine • Look for a support group • Look for care takers
Yes, it can cause memory loss in later stage of the disease. As there is a progressive loss of brain function, leading to memory loss.
One must consult a doctor who has expertise in treating disorders of brain and nerves. Look for the best neurologist in your location.
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L'infurmazioni nantu à sta pagina sò state riviste è appruvate da Mozocare squadra. Sta pagina hè stata aggiornata u Mar 31, 2022.