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Segawa syndrome, autosomal recessive

Segawa syndrome, autosomal recessive: Introduction

Segawa syndrome, autosomal recessive: A very rare birth disorder characterized mainly by involuntary jerky movements that start during infancy. The disorder is caused by a genetic defect resulting in a deficiency of an enzyme called tyrosine hydroxylase. The disorder is usually treatable by administering low doses of L-DOPA medication. More detailed information about the symptoms, causes, and treatments of Segawa syndrome, autosomal recessive is available below.

Symptoms of Segawa syndrome, autosomal recessive

Treatments for Segawa syndrome, autosomal recessive

Wrongly Diagnosed with Segawa syndrome, autosomal recessive?

Segawa syndrome, autosomal recessive: Related Patient Stories

Segawa syndrome, autosomal recessive: Complications

Read more about complications of Segawa syndrome, autosomal recessive.

Causes of Segawa syndrome, autosomal recessive

Read more about causes of Segawa syndrome, autosomal recessive.

Misdiagnosis and Segawa syndrome, autosomal recessive

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Segawa syndrome, autosomal recessive: Research Doctors & Specialists

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Segawa syndrome, autosomal recessive: Animations

Segawa syndrome, autosomal recessive: Broader Related Topics

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