Literature DB >> 17662898

Hypermelanoses of the newborn and of the infant.

Alain Taïeb1, Franck Boralevi.   

Abstract

This article discusses hypermelanoses present at birth or appearing in the first months of life. They may be transient or permanent, localized - as in café-au-lait spots - or segmental, or more rarely, complex or generalized. In most pigmentary diseases, physical examination, including Wood's lamp examination and a detailed history, is usually sufficient. Time of onset, distribution pattern, and associated clinical and sometimes histopathologic findings are helpful in differentiating these disorders. Recently, molecular diagnosis has become available for some rare entities, such as hereditary symmetrical dyschromatoses, but the bulk of nevoid lesions are not understood at the molecular level.

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Year:  2007        PMID: 17662898     DOI: 10.1016/j.det.2007.04.011

Source DB:  PubMed          Journal:  Dermatol Clin        ISSN: 0733-8635            Impact factor:   3.478


  4 in total

Review 1.  Genodermatoses caused by genetic mosaicism.

Authors:  M Vreeburg; M A M van Steensel
Journal:  Eur J Pediatr       Date:  2012-11-01       Impact factor: 3.183

Review 2.  The etiology and molecular genetics of human pigmentation disorders.

Authors:  Laura L Baxter; William J Pavan
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2012-05-17       Impact factor: 5.814

3.  Dermatologic issues in adult survivors of childhood cancer.

Authors:  Karen E Kinahan; Mona Gandhi; Mario E Lacouture; Robert Eilers; Anand Haryani; Aarati Didwania; Lisa K Sharp
Journal:  J Cancer Surviv       Date:  2009-05-28       Impact factor: 4.442

4.  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 in total

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