Literature DB >> 15340709

[Inherited metabolic disorders with cutaneous manifestations].

P Poblete-Gutiérrez1, T Wiederholt, J Frank.   

Abstract

Over the last years, the genetic basis of several monogenic inherited metabolic diseases has been elucidated. Interestingly, some of these disorders manifest with characteristic cutaneous symptoms that are often crucial for diagnosis. In most cases, however, besides the skin other organs are affected. Therefore, an interdisciplinary supervision of these patients is highly important. In this review we will discuss diseases that constitute a challenge not only for dermatologists but also for physicians from other specialties. A particular emphasis is put on genetic and clinical features of these disorders as well as current therapeutic concepts.

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Year:  2004        PMID: 15340709     DOI: 10.1007/s00105-004-0797-1

Source DB:  PubMed          Journal:  Hautarzt        ISSN: 0017-8470            Impact factor:   0.751


  15 in total

1.  Altered selectivity in an Arabidopsis metal transporter.

Authors:  E E Rogers; D J Eide; M L Guerinot
Journal:  Proc Natl Acad Sci U S A       Date:  2000-10-24       Impact factor: 11.205

Review 2.  Diagnosis and treatment of the acute porphyrias: an interdisciplinary challenge.

Authors:  P Poblete Gutiérrez; O Kunitz; C Wolff; J Frank
Journal:  Skin Pharmacol Appl Skin Physiol       Date:  2001 Nov-Dec

Review 3.  The genetic bases of the porphyrias.

Authors:  J Frank; A M Christiano
Journal:  Skin Pharmacol Appl Skin Physiol       Date:  1998 Nov-Dec

4.  Identification of SLC39A4, a gene involved in acrodermatitis enteropathica.

Authors:  Sébastien Küry; Brigitte Dréno; Stéphane Bézieau; Stéphanie Giraudet; Monia Kharfi; Ridha Kamoun; Jean-Paul Moisan
Journal:  Nat Genet       Date:  2002-06-17       Impact factor: 38.330

Review 5.  Mapping complex traits in diseases of the hair and skin.

Authors:  V M Aita; A M Christiano; T C Gilliam
Journal:  Exp Dermatol       Date:  1999-12       Impact factor: 3.960

6.  [Angiokeratoma corporis diffusum universale (Fabry disease)].

Authors:  J Frank; W Jansen-Genzel; A Lentner; V Wienert
Journal:  Hautarzt       Date:  1996-10       Impact factor: 0.751

Review 7.  Hepatic porphyrias: pathobiochemical, diagnostic, and therapeutic implications.

Authors:  M O Doss
Journal:  Prog Liver Dis       Date:  1982

Review 8.  [Mapping and molecular analysis of hereditary skin diseases. The status of current research].

Authors:  W Küster; H C Hennies; R Happle
Journal:  Hautarzt       Date:  2000-12       Impact factor: 0.751

Review 9.  Enzyme replacement and enhancement therapies for lysosomal diseases.

Authors:  R J Desnick
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

10.  Structural organization of the human alpha-galactosidase A gene: further evidence for the absence of a 3' untranslated region.

Authors:  D F Bishop; R Kornreich; R J Desnick
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

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  3 in total

1.  [Erythematous papules in a 26-year-old man].

Authors:  N Koch; F Butsch
Journal:  Hautarzt       Date:  2015-11       Impact factor: 0.751

2.  [Hereditary metabolic diseases with cutaneous manifestations : An update].

Authors:  J Frank; P Poblete-Gutiérrez
Journal:  Hautarzt       Date:  2011-02       Impact factor: 0.751

3.  [Transient zinc deficiency in preterm infants].

Authors:  F Benedix; U Hermann; C Brod; G Metzler; C Sönnichsen; M Röcken; M Schaller
Journal:  Hautarzt       Date:  2008-07       Impact factor: 0.751

  3 in total

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