Literature DB >> 454568

Keratosis pilaris atrophicans faciei (ulerythema ophryogenes): a cutaneous marker in the Noonan syndrome.

D O Pierini, A M Pierini.   

Abstract

Five cases are reported of Noonan's syndrome, all of which presented keratosis pilaris atrophicans faciei (ulerythema ophryogenes). This dermatosis fulfils the criteria mentioned by Noonan & Ehmke (1963) as a pointer for the investigation of cardiac anomalies, especially of the pulmonary artery.

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Year:  1979        PMID： 454568     DOI： 10.1111/j.1365-2133.1979.tb01641.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


  7 in total

1.  The genes for Noonan's syndrome, woolly hair and ulerythema ophryogenes.

Authors:  J L Burton
Journal:  Postgrad Med J       Date:  1992-07       Impact factor: 2.401

2.  A clinical study of Noonan syndrome.

Authors:  M Sharland; M Burch; W M McKenna; M A Paton
Journal:  Arch Dis Child       Date:  1992-02       Impact factor: 3.791

3.  A Noonan-like short stature syndrome with sparse hair.

Authors:  M Baraitser; M A Patton
Journal:  J Med Genet       Date:  1986-04       Impact factor: 6.318

Review 4.  Noonan syndrome.

Authors:  J E Allanson
Journal:  J Med Genet       Date:  1987-01       Impact factor: 6.318

Review 5.  Noonan syndrome.

Authors:  Ineke van der Burgt
Journal:  Orphanet J Rare Dis       Date:  2007-01-14       Impact factor: 4.123

6.  Ulerythema ophryogenes in association with MAP3K1-mutated Swyer syndrome.

Authors:  Ila Nimgaonkar; Marielle Jamgochian; David M Milgraum; Amy S Pappert; Sandy S Milgraum
Journal:  JAAD Case Rep       Date:  2022-05-21

Review 7.  The other side of Turner's: Noonan's syndrome.

Authors:  Pankaj Agarwal; Rajeev Philip; Manish Gutch; K K Gupta
Journal:  Indian J Endocrinol Metab       Date:  2013-09
  7 in total

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