Literature DB >> 1377724

An association of acanthosis nigricans and Crouzon syndrome.

H Koizumi1, T Tomoyori, K C Sato, A Ohkawara.   

Abstract

An 11-year-old Japanese female having acanthosis nigricans associated with Crouzon syndrome is reported. Crouzon syndrome is a craniostenotic craniofacial malformation associated with premature closure of selective calvarial sutures, exophthalmos, maxillary hypoplasia, and a beak-shaped nose. It is an autosomal dominant inherited disorder. Crouzon syndrome is one of the syndromes which may be associated with acanthosis nigricans. The association of acanthosis nigricans with Crouzon syndrome is assumed to be a rare abnormality, although the true frequency is uncertain. We have reviewed the reported cases of acanthosis nigricans associated with Crouzon syndrome and characteristics were discussed.

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Year:  1992        PMID: 1377724     DOI: 10.1111/j.1346-8138.1992.tb03193.x

Source DB:  PubMed          Journal:  J Dermatol        ISSN: 0385-2407            Impact factor:   4.005


  2 in total

1.  A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans.

Authors:  D Wilkes; P Rutland; L J Pulleyn; W Reardon; C Moss; J P Ellis; R M Winter; S Malcolm
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318

2.  Crouzon syndrome with acanthosis nigricans: a case-based update.

Authors:  Federico Di Rocco; Corinne Collet; Laurence Legeai-Mallet; Eric Arnaud; Martine Le Merrer; Smail Hadj-Rabia; Dominique Renier
Journal:  Childs Nerv Syst       Date:  2010-12-07       Impact factor: 1.475

  2 in total

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