| Literature DB >> 26212801 |
María Lía Pieretti1, Rebeca Alcalá2, Paula Boggio1, Lucero Noguera-Morel2, María Librada Porriño3, Paula C Luna4, Angela Hernández-Martín2, Roberto Schroh5, Margarita Larralde1,4, Antonio Torrelo2.
Abstract
Aplasia cutis congenita (ACC), or congenital absence of skin, is a heterogeneous condition that may be due to varied mechanisms. ACC has rarely been reported in association with fetus papyraceus, representing a peculiar phenotype of ACC. We present six new cases of neonates born with symmetric ACC associated with intrauterine fetal demise of co-twins during the late first or early second trimester.Entities:
Mesh：
Year: 2015 PMID： 26212801 DOI： 10.1111/pde.12651
Source DB: PubMed Journal: Pediatr Dermatol ISSN： 0736-8046 Impact factor: 1.588