MITOSWAB™ — is a unique tool used to diagnose mitochondrial dysfunction.

What is MitoSWAB™ (MitoSwab)?

MitoSWAB™ Plus is the first and only «non-invasive» assessment test for the study of mitochondrial dysfunction, analyzing components of the electron transport chain – complex I, II, III, and IV.

Why does it matter?
Mitochondrial disorders can occur at any age and in most cases affect both sexes equally.
Knowing the functional capacity of the mitochondria is vital to managing overall health. An effective assessment of the impairment can help initiate treatment in time.

What are the signs and symptoms of mitochondrial diseases?

  • fatigue;
  • growth retardation;
  • learning problems;
  • physical activity intolerance;
  • muscle weakness;
  • loss of muscle coordination;
  • neurological symptoms;
  • gastrointestinal symptoms;
  • heart failure;
  • deafness;
  • blindness.

What happens when mitochondria don't function properly?
Studies show that mitochondrial dysfunction can be a prerequisite for many neurological disorders. Also, clinical signs of mitochondrial disorders can involve either a single organ or any combination of organ systems. 

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Mitochondrial dysfunction manifests itself as follows:

  • autism spectrum disorder ASD;
  • Parkinson's disease;
  • dementia;
  • bipolar disorder;
  • schizophrenia;
  • depression;
  • diabetes mellitus;
  • asthma;
  • chronic fatigue syndrome;
  • cramps;
  • gastrointestinal problems;
  • heart and kidney problems;
  • mitochondrial disease;
  • Ley's disease;
  • Leber hereditary optical neuropathy (LHON);
  • autosomal dominant optic atrophy (ADOA);
  • pyruvate dehydrogenase deficiency;
  • other genetic disorders such as Alpers syndrome, Bart's syndrome, carnitine deficiency, complex I, II, III, IV, V deficiency, coenzyme Q10 deficiency, MELAS, etc.

How does the MITOSWAB test help you? 

MITOSWAB™ is a unique tool that is used to diagnose mitochondrial dysfunction. It is also a valuable method that can be used to monitor the effectiveness of prescribed therapy. MITOSWAB™ has an 84% correlation with muscle biopsy, which is considered the gold standard for diagnosing mitochondrial dysfunction. However, muscle biopsy is invasive (painful and difficult). MITOSWAB™ is an excellent alternative as a potential first-line test for mitochondrial dysfunction.

How is the test done?
The test is done with an oral swab (the inside of the cheeks – left and right). It is a simple procedure that is quick and easy to perform. You can do the sampling at home at your convenience. You can perform the procedure in our clinic or we can send you a kit with instructions for convenient biomaterial sampling at home. 

How to prepare for the analysis?
If you are taking certain medications on an ongoing basis, please consult your physician for advice. Because some medications/supplements can interfere with mitochondrial function.

1 hour before taking the material, clean the mouth by gently rinsing it with plain water (if the child is not able to rinse his mouth, then just let him drink water). Make sure there is no food. Wait 30 minutes if you have brushed your teeth.

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Лікуємо нашого хлопчика і бачимо позитивні результати, хлопчик став краще розмовляти, з'явився апетит, з'явилось бажання пробувати нові продукти, легше реагує на все, легше домовлятися. Дякую лікарю Володимиру Михайловичу Стефанишину.

Юрій

В клинике уютно и светло. Приятно удивляет всегда быстрое реагирование на вопросы и просьбы девушек-регистраторов, их доброжелательное отношение. Ни один вопрос в вайбере не остался без ответа. Дважды были с сыном на консультации у Шейко Макара Васильевича. Неординарный, профессиональный и, в то же время, душевный, можно сказать дружеский подход, к решению проблем пациента, у Макара Васильевича. Также 2 года назад мы были на приеме у иммунолога Мельник Леси Игоревны. Остались тоже очень довольны. Впечатлило глубокое понимание проблемы, а также достаточно доступное объяснение и интересное изложение информации.

Елена Моцарь

Доброго дня! Нарешті я написала відгук, вже півроку з вами) Я мама дитини, яка до 18 років мала купу діагнозів, які і близько не мали відношення до нашої хвороби! Уявіть, скільки часу було витрачено... лікування ніяке (звісно) не допомагало, а ставало ще гірше. Доки нам не порекомендували Шейко Макар Васильовича! Сказати, що Він нам допоміг , це нічого не сказати! Макар Васильович врятував мою Софію! Завдяки правильній діагностиці, ми маємо НАШ діагноз (рідке орфанне захворювання) і правильне лікування. Я бачу поліпшення, моя дитина як заново народилася! Макар Васильович - це дбайлива і дуже чутна Людина, якій довіряєш! На прийомі немає оцього бар'єру лікар-пацієнт, ви як прийшли до друга, який вас підбадьорить, вислухає. Дуже рекомендую!

Анна

По аналізам у дитини герпес 6 типу, звернулись в клініку до імунолога Лесі Мельник на консультацію, лікар професійно все пояснила та назначила курс лікування.

Наталія

Дуже задоволений фаховим спеціалістом Монастирським В. О. Спеціаліст вищої категорії з величезним досвідом лікування. Уважний, компетентний, фаховий невропатолог, нейроімунолог. Моя подяка Володимиру Олеговичу.

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