GM1 Gangliosidosis Type 1 and Mongolian Spots

J Gordon Millichap

doi:10.15844/pedneurbriefs-27-6-10

GM1 Gangliosidosis Type 1 and Mongolian Spots

Pediatric Neurology Briefs

Volume 27 (2013): Issue 6

By: J Gordon Millichap

Open Access

|Jun 2013

Abstract

Investigators in Sao Paulo, Brazil, report a female infant born at term to healthy consanguineous parents who was examined at 9 months for delayed development.

References

Hackbart BA Arita JH Pinho RS Masruha MR Vilanova LC Mongolian spots are not always a benign sign J Pediatr 2013 May 162 5 1070 10.1016/j.jpeds.2012.12.044 23374678
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Weissbluth M Esterly NB Caro WA Report of an infant with GM1 gangliosidosis type I and extensive and unusual mongolian spots Br J Dermatol 1981 Feb 104 2 195 200 10.1111/j.1365-2133.1981.tb00045.x 6783061
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Ashrafi MR Shabanian R Mohammadi M Kavusi S Extensive Mongolian spots: a clinical sign merits special attention Pediatr Neurol 2006 Feb 34 2 143 5 10.1016/j.pediatrneurol.2005.07.010 16458829
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-27-6-10 | Journal eISSN: 2166-6482

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Language: English

Page range: 47 - 48

Published on: Jun 1, 2013

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Hepatosplenomegaly,

GM1 Gangliosidosis Type 1,

Lysosomal Disease

© 2013 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 27 (2013): Issue 6