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Tyrosinaemia type 2

Introduction: Tyrosinaemia type 2

Description of Tyrosinaemia type 2

Tyrosinaemia type 2: An inborn error of amino acid metabolism characterized by keratosis palmaris et plantaris, persistent dendritic lesions of the cornea with unaffected corneal sensitivity, photophobia, and persistent tearing in association with tyrosine aminotransaminase deficiency and elevated blood tyrosine level. Severe mental and somatic retardation occur in most cases. Visual complications may include blindness.
Source: Diseases Database

Tyrosinaemia type 2: Related Topics

These medical condition or symptom topics may be relevant to medical information for Tyrosinaemia type 2:

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Terms Similar to Tyrosinaemia type 2:

Source: Diseases Database

External links related to: Tyrosinaemia type 2

Source: Diseases Database

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