Literature DB >> 21739579

A pigmentary skin defect is a new finding in Marshall-Smith syndrome.

Cristóbal Passalacqua1, Camila Melo, Luz María Martín, Francisca Rojas, Patricia Sanz, Silvia Castillo Taucher, Ligia Aranibar.   

Abstract

Marshall-Smith Syndrome (OMIM 602535) was described initially by Marshall in two infants with a syndrome characterized by accelerated skeletal maturation, failure to thrive, and dysmorphic facial features. We report a new patient with clinical features of Marshall-Smith syndrome with additional findings such as hyperpigmented lines on trunk and the four extremities. © 2011 Wiley-Liss, Inc.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21739579     DOI: 10.1002/ajmg.a.34076

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  1 in total

1.  Marshall-Smith syndrome.

Authors:  T E Herman; M J Siegel
Journal:  J Perinatol       Date:  2015-04       Impact factor: 2.521

  1 in total

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