Abstract
These skin diseases are usually the result of a congenital deficiency of enzymes which catalyze the synthesis or transport of specific amino acids. Disorders of amino acid metabolism manifest themselves in cutaneous organs as anomalies of the pigmentation of skin and hair, in structural disorders of the hair, and in some cases in pellagroid symptoms. In patients with congenital structural disorders of the hair it is important to remember disorders of amino acid metabolism and to have amino acid assays carried out on blood or urine.
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Bibliography: Skin Diseases Due to Disorders of Amino Acid Metabolism
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© 1991 Springer-Verlag Berlin Heidelberg
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Braun-Falco, O., Plewig, G., Wolff, H.H., Winkelmann, R.K. (1991). Skin Diseases Due to Disorders of Amino Acid Metabolism. In: Dermatology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-00181-3_39
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DOI: https://doi.org/10.1007/978-3-662-00181-3_39
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