Association D’Une Hemochromatose Idiopathique Et D’Une Porphyrie Cutanee Tardive
作者:
BuysschaertM.,
VerstraetenL.,
NovikV.,
BrasseurA.,
DonckierJ.,
HassounA.,
期刊:
Acta Clinica Belgica
(Taylor Available online 1991)
卷期:
Volume 46,
issue 5
页码: 333-337
ISSN:1784-3286
年代: 1991
DOI:10.1080/17843286.1991.11718185
出版商: Taylor&Francis
数据来源: Taylor
摘要:
SummaryPorphyria cutanea tarda is a disorder of porphyrin metabolism that results from a deficiency of uroporphyrinogen decarboxylase, resulting in a characteristic pattern of porphyrin excretion. Elevated serum iron values are frequently observed among patients with porphyria cutanea tarda. The hypothesis has been advanced that a hemochromatosis allele is implicated in the clinical manifestation of porphyria cutanea tarda. We report the case of a patient suffering from both idiopathic hemochromatosis and porphyria cutanea tarda. The data of the medical literature concerning such an association are discussed.
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