Zinc therapy of neurological Wilson’s disease in a woman with two foetus with agenesis of the corpus callosum

CLINICAL REPORT: A patient diagnosed Wilson’s disease (WD) 22 years previously, successfully tre­ated initially with zinc, developed neuropsychiatric disease after years of irregular therapy. Reassuming zinc therapy was successful. After a normal pregnancy, she had two therapeutic abortions for corpus callosum agenesis, and a missed abortion. We review the genetics, physiopathology, clinics and imagiologic response to zinc therapy, the problems of pregnancy in WD, advising to maintain therapy. A hypothetic cause for fetus brain anomaly would be hypocupremia due to zinc therapy, confronting with two other possibilities, one related to Wilson’s disease in itself, other due to a congenital syndrome of agenesis of the corpus callosum, impossible to diagnose by our available diagnostic methods.

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Main Authors: Murinello,António, Tomé,Teresa, Goulão,Augusto, Cohen,Álvaro
Format: Digital revista
Language:English
Published: Sociedade Portuguesa de Gastrenterologia 2010
Online Access:http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-81782010000300005
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spelling oai:scielo:S0872-817820100003000052010-12-28Zinc therapy of neurological Wilson’s disease in a woman with two foetus with agenesis of the corpus callosumMurinello,AntónioTomé,TeresaGoulão,AugustoCohen,Álvaro Wilson’s disease zinc corpus callosum agenesis hypocupremia CLINICAL REPORT: A patient diagnosed Wilson’s disease (WD) 22 years previously, successfully tre­ated initially with zinc, developed neuropsychiatric disease after years of irregular therapy. Reassuming zinc therapy was successful. After a normal pregnancy, she had two therapeutic abortions for corpus callosum agenesis, and a missed abortion. We review the genetics, physiopathology, clinics and imagiologic response to zinc therapy, the problems of pregnancy in WD, advising to maintain therapy. A hypothetic cause for fetus brain anomaly would be hypocupremia due to zinc therapy, confronting with two other possibilities, one related to Wilson’s disease in itself, other due to a congenital syndrome of agenesis of the corpus callosum, impossible to diagnose by our available diagnostic methods.info:eu-repo/semantics/openAccessSociedade Portuguesa de GastrenterologiaJornal Português de Gastrenterologia v.17 n.3 20102010-05-01info:eu-repo/semantics/reporttext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-81782010000300005en
institution SCIELO
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country Portugal
countrycode PT
component Revista
access En linea
databasecode rev-scielo-pt
tag revista
region Europa del Sur
libraryname SciELO
language English
format Digital
author Murinello,António
Tomé,Teresa
Goulão,Augusto
Cohen,Álvaro
spellingShingle Murinello,António
Tomé,Teresa
Goulão,Augusto
Cohen,Álvaro
Zinc therapy of neurological Wilson’s disease in a woman with two foetus with agenesis of the corpus callosum
author_facet Murinello,António
Tomé,Teresa
Goulão,Augusto
Cohen,Álvaro
author_sort Murinello,António
title Zinc therapy of neurological Wilson’s disease in a woman with two foetus with agenesis of the corpus callosum
title_short Zinc therapy of neurological Wilson’s disease in a woman with two foetus with agenesis of the corpus callosum
title_full Zinc therapy of neurological Wilson’s disease in a woman with two foetus with agenesis of the corpus callosum
title_fullStr Zinc therapy of neurological Wilson’s disease in a woman with two foetus with agenesis of the corpus callosum
title_full_unstemmed Zinc therapy of neurological Wilson’s disease in a woman with two foetus with agenesis of the corpus callosum
title_sort zinc therapy of neurological wilson’s disease in a woman with two foetus with agenesis of the corpus callosum
description CLINICAL REPORT: A patient diagnosed Wilson’s disease (WD) 22 years previously, successfully tre­ated initially with zinc, developed neuropsychiatric disease after years of irregular therapy. Reassuming zinc therapy was successful. After a normal pregnancy, she had two therapeutic abortions for corpus callosum agenesis, and a missed abortion. We review the genetics, physiopathology, clinics and imagiologic response to zinc therapy, the problems of pregnancy in WD, advising to maintain therapy. A hypothetic cause for fetus brain anomaly would be hypocupremia due to zinc therapy, confronting with two other possibilities, one related to Wilson’s disease in itself, other due to a congenital syndrome of agenesis of the corpus callosum, impossible to diagnose by our available diagnostic methods.
publisher Sociedade Portuguesa de Gastrenterologia
publishDate 2010
url http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-81782010000300005
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AT goulaoaugusto zinctherapyofneurologicalwilsonsdiseaseinawomanwithtwofoetuswithagenesisofthecorpuscallosum
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