multiple mitochondrial dysfunctions syndrome 9b

A mitochondrial dysfunction syndrome in which the cause of the disease is a mutation in the FDXR gene. It is characterized by optic atrophy and/or auditory neuropathy variably associated with developmental delay or regression, global hypotonia, pyramidal and cerebellar signs, and seizures.

What is multiple mitochondrial dysfunctions syndrome 9b?

multiple mitochondrial dysfunctions syndrome 9b is a medical condition. A condition is a disease, disorder, or abnormal state that affects the body or mind. This page provides educational information only and is not a diagnosis.

If you think you may have multiple mitochondrial dysfunctions syndrome 9b, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with multiple mitochondrial dysfunctions syndrome 9b

Abdominal painAnxietyAstheniaAxial muscle weaknessBlindnessBlurred visionConstipationCoughDepressionDistal lower limb muscle weaknessDrowsinessDysphagia

When to seek medical care

Seek medical advice if you have symptoms that are severe, persistent, or affecting your daily life. Emergency care is needed for symptoms like chest pain, difficulty breathing, confusion, or severe weakness.