Hanhart Syndrome natural cures

Hanhart Syndrome Definition

Hanhart syndrome otherwise known as the Richner Syndrome, is an autosomal recessive disorder caused by deficiency in enzyme tyrosine amono transferase (E. Hanhart: ?ber die Kombination von Peromelia mit Mikrognathia, ein neues Syndrom beim Menschen, entsprechend der Akroteriasis congenita von Wriedt und Mohr beim Rinde. Archiv der Julius Klaus-Stiftung f?r Vererbungsforschung, Sozialanthropologie und Rassenhygiene, Z?rich, 1950, 25: 531-544).

Hanhart Syndrome Diagnosis

Diagnosis includes medical and laboratory examinations including clinical tests to determine the enzyme tyrosine amino transferase in the body.

Hanhart Syndrome Treatment

Treatment includes restriction of amino acids phenylalanine and tyrosine in take.

Hanhart Syndrome Symptoms and Signs

Symptoms include ocular lesions and palmoplanter hyperkeratosis. Eye symptoms include redness, lacrimaton and photophobis.

Hanhart Syndrome Causes
It said to be a caused of the deficiency in enzyme tyrosine amino transferase.

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