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[A rare metabolic disease: alkaptonuria--ochronosis].

作者信息

Hortobágyi J, Schneider I, Sebök B, Klujber L

机构信息

Dermatologische Klinik, Medizinischen Universität Pécs.

出版信息

Hautarzt. 1992 Sep;43(9):580-2.

PMID:1328117
Abstract

The authors describe the case of a 40-year-old female patient. Since childhood her urine had caused black discoloration on her underwear. For about a year the skin of the axillae and pinnae had been bluish-black without subjective complaints. One year before admission, pain in the thoracic and lumbar spine began, with limitation of motion. Examination of the urine, histological and electron microscopical findings, and X-ray examination of the spinal column confirmed the diagnosis of alkaptonuria and congenital ochronosis.

摘要

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