Clinical Remission of Delta-Aminolevulinic Acid Dehydratase Deficiency through Suppression of Erythroid Heme Synthesis

Rochus A Neeleman; Eduard J van Beers; Edith C Friesema; Rita Koole-Lesuis; Willem L van der Pol; J H Paul Wilson; Janneke G Langendonk

doi:10.1002/hep.30543

Clinical Remission of Delta-Aminolevulinic Acid Dehydratase Deficiency through Suppression of Erythroid Heme Synthesis

Rochus A Neeleman
, Eduard J van Beers
, Edith C Friesema
, Rita Koole-Lesuis
, Willem L van der Pol
, J H Paul Wilson
, Janneke G Langendonk

Hematology/Van Creveldclinic

Research output: Contribution to journal › Editorial › Academic › peer-review

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Abstract

We present a case of delta-aminolevulinic acid dehydratase-porphyria (ADP) who was successfully treated by suppressing bone-marrow production of toxic heme precursors. Together with supporting evidence from earlier cases, it is likely ADP has both hepatic and erythroid origins. This article is protected by copyright. All rights reserved.

Original language	English
Pages (from-to)	434-436
Number of pages	3
Journal	Hepatology (Baltimore, Md.)
Volume	70
Issue number	1
Early online date	6 Feb 2019
DOIs	https://doi.org/10.1002/hep.30543
Publication status	Published - Jul 2019

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title = "Clinical Remission of Delta-Aminolevulinic Acid Dehydratase Deficiency through Suppression of Erythroid Heme Synthesis",

abstract = "We present a case of delta-aminolevulinic acid dehydratase-porphyria (ADP) who was successfully treated by suppressing bone-marrow production of toxic heme precursors. Together with supporting evidence from earlier cases, it is likely ADP has both hepatic and erythroid origins. This article is protected by copyright. All rights reserved.",

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AU - Neeleman, Rochus A

AU - van Beers, Eduard J

AU - Friesema, Edith C

AU - Koole-Lesuis, Rita

AU - van der Pol, Willem L

AU - Wilson, J H Paul

AU - Langendonk, Janneke G

PY - 2019/7

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N2 - We present a case of delta-aminolevulinic acid dehydratase-porphyria (ADP) who was successfully treated by suppressing bone-marrow production of toxic heme precursors. Together with supporting evidence from earlier cases, it is likely ADP has both hepatic and erythroid origins. This article is protected by copyright. All rights reserved.

AB - We present a case of delta-aminolevulinic acid dehydratase-porphyria (ADP) who was successfully treated by suppressing bone-marrow production of toxic heme precursors. Together with supporting evidence from earlier cases, it is likely ADP has both hepatic and erythroid origins. This article is protected by copyright. All rights reserved.

UR - https://www.scopus.com/pages/publications/85067074355

U2 - 10.1002/hep.30543

DO - 10.1002/hep.30543

M3 - Editorial

C2 - 30724374

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VL - 70

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JO - Hepatology (Baltimore, Md.)

JF - Hepatology (Baltimore, Md.)

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ER -

Clinical Remission of Delta-Aminolevulinic Acid Dehydratase Deficiency through Suppression of Erythroid Heme Synthesis

Abstract

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