Ernst Hanhart (1891-1973 ) and the syndrome which bears his name

Richner-Hanhart syndrome (RHS) is a rare autosomal recessive disease associated with high serum tyrosine levels .RHS is caused by the deficiency of tyrosine aminotransferase enzyme (TAT) [1-5]. RHS should be suspected in patients demonstrating dermatologic signs, especially palmoplantar keratosis, a...

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Published inNasza dermatologia online Vol. 4; no. 1; pp. 106 - 107
Main Author Al Aboud, Ahmad
Format Journal Article
LanguageEnglish
Published Slupsk Our Dermatology Online 01.01.2013
Subjects
Ernst Hanhart
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Summary:Richner-Hanhart syndrome (RHS) is a rare autosomal recessive disease associated with high serum tyrosine levels .RHS is caused by the deficiency of tyrosine aminotransferase enzyme (TAT) [1-5]. RHS should be suspected in patients demonstrating dermatologic signs, especially palmoplantar keratosis, associated with bilateral pseudodendritic corneal lesions unresponsive to antiviral therapy [1].
ISSN:2081-9390
2081-9390
DOI:10.7241/ourd.20131.26