Literature DB >> 31076812

[Pigmented macules as possible early signs of genetic syndromes].

H Hamm1, K Emmerich2, J Olk2.   

Abstract

Solitary congenital or early apparent pigmented macules are usually without relevance; however, when multiple, extensive or in a patterned arrangement, they are not uncommonly the first sign of an underlying genetic syndrome. The present article gives an overview on the clinical significance of multiple café-au-lait macules, multiple lentigines and pigmentary mosaicism and discusses the differential diagnosis of associated syndromes. Early diagnosis with the essential contribution of the dermatologist is not only important for genetic counseling but can also contribute to avoidance of sometimes life-threatening complications.

Entities:  

Keywords:  Cafe-au-lait spots; Genetic disorders; Hyperpigmentation; Lentigines; Pigmentary mosaicism

Mesh:

Year:  2019        PMID: 31076812     DOI: 10.1007/s00105-019-4416-6

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


  29 in total

1.  Somatic mutation analysis in NF1 café au lait spots reveals two NF1 hits in the melanocytes.

Authors:  Sofie De Schepper; Ophélia Maertens; Tom Callens; Jean-Marie Naeyaert; Jo Lambert; Ludwine Messiaen
Journal:  J Invest Dermatol       Date:  2007-10-04       Impact factor: 8.551

Review 2.  The diagnostic value of café-au-lait macules.

Authors:  M Landau; B R Krafchik
Journal:  J Am Acad Dermatol       Date:  1999-06       Impact factor: 11.527

3.  Segmental pigmentation disorder.

Authors:  M Hogeling; I J Frieden
Journal:  Br J Dermatol       Date:  2010-02-15       Impact factor: 9.302

Review 4.  Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis.

Authors:  Anke Hartmann; Uta B Hofmann; Holger Hoehn; Eva B Broecker; Henning Hamm
Journal:  Pediatr Dermatol       Date:  2004 Nov-Dec       Impact factor: 1.588

5.  Between light and dark, the chimera comes out.

Authors:  Dan Lipsker; Elisabeth Flory; Marie-Louise Wiesel; Daniel Hanau; Henri de la Salle
Journal:  Arch Dermatol       Date:  2008-03

Review 6.  Neurofibromatosis type 1.

Authors:  Kevin P Boyd; Bruce R Korf; Amy Theos
Journal:  J Am Acad Dermatol       Date:  2009-07       Impact factor: 11.527

Review 7.  Carney complex and lentiginosis.

Authors:  Anelia Horvath; Constantine A Stratakis
Journal:  Pigment Cell Melanoma Res       Date:  2009-07-24       Impact factor: 4.693

8.  Predictive value of café au lait macules at initial consultation in the diagnosis of neurofibromatosis type 1.

Authors:  Kara S Nunley; Feng Gao; Anne C Albers; Susan J Bayliss; David H Gutmann
Journal:  Arch Dermatol       Date:  2009-08

9.  Linear and whorled hypermelanosis.

Authors:  Vito Di Lernia
Journal:  Pediatr Dermatol       Date:  2007 May-Jun       Impact factor: 1.588

Review 10.  Leopard syndrome.

Authors:  Anna Sarkozy; Maria Cristina Digilio; Bruno Dallapiccola
Journal:  Orphanet J Rare Dis       Date:  2008-05-27       Impact factor: 4.123

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