Literature DB >> 12873889

Association of dermal melanocytosis with lysosomal storage disease: clinical features and hypotheses regarding pathogenesis.

Miriam Hanson1, James R Lupski, John Hicks, Denise Metry.   

Abstract

BACKGROUND: The potential association of dermal melanocytosis with lysosomal storage disease in infancy is an uncommonly known and poorly understood entity. OBSERVATIONS: We describe 2 infants with extensive dermal melanocytosis in association with GM1 gangliosidosis type 1 and Hurler syndrome, respectively. A literature analysis revealed 37 additional cases. Clinically, dermal melanocytosis associated with lysosomal storage disease is characterized by extensive, blue cutaneous pigmentation with dorsal and ventral distribution, indistinct borders, and persistent and/or "progressive" behavior. GM1 gangliosidosis type 1 and Hurler syndrome are the most common underlying disorders associated with these cutaneous features.
CONCLUSIONS: In the appropriate clinical setting, an unusual presentation of dermal melanocytosis in an infant may be a cutaneous sign of an underlying lysosomal storage disease. The pathogenetic mechanisms behind this association remain to be elucidated.

Entities:  

Mesh:

Year:  2003        PMID: 12873889     DOI: 10.1001/archderm.139.7.916

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  11 in total

Review 1.  A comprehensive review of Mongolian spots with an update on atypical presentations.

Authors:  Yusuf Alimi; Joe Iwanaga; Marios Loukas; Rod J Oskouian; Elias Rizk; W Jerry Oakes; R Shane Tubbs
Journal:  Childs Nerv Syst       Date:  2018-08-06       Impact factor: 1.475

2.  Mongolian spots: How important are they?

Authors:  Divya Gupta; Devinder Mohan Thappa
Journal:  World J Clin Cases       Date:  2013-11-16       Impact factor: 1.337

3.  Extensive mongolian spots with autosomal dominant inheritance.

Authors:  Yc Beeregowda; Kumar Bv Naveen; Yc Manjunatha
Journal:  Iran J Pediatr       Date:  2012-06       Impact factor: 0.364

4.  Gm1 gangliosidosis associated with neonatal-onset of diffuse ecchymoses and mongolian spots.

Authors:  Imad Dweikat; Bassam Abu Libdeh; Hanadi Murrar; Samir Khalil; Nizar Maraqa
Journal:  Indian J Dermatol       Date:  2011-01       Impact factor: 1.494

5.  Glycosaminoglycan storage disorders: a review.

Authors:  Maria Francisca Coutinho; Lúcia Lacerda; Sandra Alves
Journal:  Biochem Res Int       Date:  2011-10-05

Review 6.  Clinical and biochemical footprints of inherited metabolic diseases. VI. Metabolic dermatoses.

Authors:  Carlos R Ferreira; Diego Martinelli; Nenad Blau
Journal:  Mol Genet Metab       Date:  2021-07-21       Impact factor: 4.204

7.  Hurler's Disease with Multiple Atypical Mongolian Spots.

Authors:  Sidharth Sonthalia; Rashmi Khurana
Journal:  Indian J Dermatol       Date:  2016 Mar-Apr       Impact factor: 1.494

8.  Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis.

Authors:  Anna C Thomas; Zhiqiang Zeng; Jean-Baptiste Rivière; Ryan O'Shaughnessy; Lara Al-Olabi; Judith St-Onge; David J Atherton; Hélène Aubert; Lorea Bagazgoitia; Sébastien Barbarot; Emmanuelle Bourrat; Christine Chiaverini; W Kling Chong; Yannis Duffourd; Mary Glover; Leopold Groesser; Smail Hadj-Rabia; Henning Hamm; Rudolf Happle; Imran Mushtaq; Jean-Philippe Lacour; Regula Waelchli; Marion Wobser; Pierre Vabres; E Elizabeth Patton; Veronica A Kinsler
Journal:  J Invest Dermatol       Date:  2016-01-14       Impact factor: 8.551

9.  Extensive Mongolian Spots in a Hypotonic Infant with GM1 Gangliosidosis.

Authors:  Suprabhat Ranjan; Pratap K Patra
Journal:  J Pediatr Neurosci       Date:  2018 Jul-Sep

Review 10.  Mucopolysaccharidosis Type I.

Authors:  Francyne Kubaski; Fabiano de Oliveira Poswar; Kristiane Michelin-Tirelli; Ursula da Silveira Matte; Dafne D Horovitz; Anneliese Lopes Barth; Guilherme Baldo; Filippo Vairo; Roberto Giugliani
Journal:  Diagnostics (Basel)       Date:  2020-03-16
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