Sialidosis type II

Sialidosis type II: Introduction

Sialidosis type II: A very rare inherited metabolic disorder where a defect in the enzyme alpha-neuraminidase prevents glycoproteins being metabolized - a severe form of Sialidosis type I. More detailed information about the symptoms, causes, and treatments of Sialidosis type II is available below.

Symptoms of Sialidosis type II

• Cherry-red ocular spot
• Impaired vision
• Night blindness
• Involuntary muscle contractions
• Impaired ability to control voluntary movements
• more symptoms...»

See full list of 14 symptoms of Sialidosis type II

Wrongly Diagnosed with Sialidosis type II?

• Misdiagnosis of Sialidosis type II

Sialidosis type II: Deaths

Read more about Deaths and Sialidosis type II.

Causes of Sialidosis type II

Read more about causes of Sialidosis type II.

Disease Topics Related To Sialidosis type II

Research the causes of these diseases that are similar to, or related to, Sialidosis type II:

• Alpha-N-acetylneuraminadse deficiency
• Myoclonic epilepsies
• Corneal opacity
• Hepatosplenomegaly
• Macular cherry spots
• more related diseases...»

Sialidosis type II: Broader Related Topics

• Genetic conditions
• Metabolic conditions
• Congenital conditions - metabolic disorders
• more types...»

Types of Sialidosis type II

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