Literature DB >> 12132297

[Multiple lentigines (LEOPARD) syndrome. Case reports and review of the literature].

G Petter1, M Rytter, U F Haustein.   

Abstract

The rarely occurring multiple lentigines (LEOPARD) syndrome represents a complex of skin, heart, skeleton and other malformations and is described in a 36-year-old male and his 9-year-old daughter. With the occurrence of multiple lentigines, the diagnostic search for further malformations should always be undertaken. Its differential diagnosis and its pathogenetic and clinical aspects are discussed in this paper.

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Year:  2002        PMID: 12132297     DOI: 10.1007/s001050100272

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


  3 in total

1.  [Sensorineural hearing loss in LEOPARD syndrome].

Authors:  T Schrom; A Habermann; H Scherer
Journal:  HNO       Date:  2006-03       Impact factor: 1.284

2.  [Molecular genetic mutation analysis of the PTPN11 gene in the multiple lentigines (LEOPARD) syndrome].

Authors:  U G Froster; H-J Glander; W Heinritz
Journal:  Hautarzt       Date:  2003-12       Impact factor: 0.751

3.  [Leukonychia totalis].

Authors:  G Wagner; V Meyer; M M Sachse
Journal:  Hautarzt       Date:  2016-04       Impact factor: 0.751

  3 in total

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