Literature DB >> 7501552

Extensive symmetric truncal aplasia cutis congenita without fetus papyraceus or macroscopic evidence of placental abnormalities.

M del C Boente1, M del V Frontini, M I Acosta, C Saleme, S Barrionuevo, R Asial.   

Abstract

Aplasia cutis congenita is a rare disorder characterized by localized absence of skin at birth. Type V in Frieden's classification, which is associated with fetus papyraceous or placental infarcts, occurs as a large cutaneous defect on the trunk and extremities. The patient we report had a lesion affecting the trunk and extremities symmetrically, with no family history of the disorder or chromosomal abnormalities. In our opinion, despite the absence of fetus papyraceous or placental infarct, this patient's condition can be classified as type V.

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Year:  1995        PMID: 7501552     DOI: 10.1111/j.1525-1470.1995.tb00164.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  1 in total

1.  A case of systemic aplasia cutis congenita: a newly recognized syndrome?

Authors:  Tokio Sugiura; Masanori Kouwaki; Shusuke Kiyosawa; Yoshie Sasada; Matsuyoshi Maeda; Kenji Goto; Norihisa Koyama
Journal:  Eur J Pediatr       Date:  2007-05-23       Impact factor: 3.183

  1 in total

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