Case report of harlequin ichthyosis who had similar history in two earlier siblings
DOI:
https://doi.org/10.66344/jpad.24.4.2014.232References
Rodriguez-Pazos L, Ginarte M, Vega A et al. Autosomal recessive congenital ichthyosis. Actas Dermosifilioger. 2013;104:270-84.
Murphy-Brown L, Vella JA, Lawlor-Klean P. Harlequin ichthyosis: a case study. Neonatal Netw. 2004;23:7-12.
Akiyama, M. The pathogenesis of severe congenital ichthyosis of the neonate. J Dermatol Sci. 1999;21:96-104.
Habib A, Pasha W, Raza N et al. Harlequin ichthyosis in two siblings. J Coll Physicians Surg Pak. 2011:21:505-5.
Peterson H, Lofgren S, Bremmer S, Krol A. Novel ABCA-12 mutations leading to recessive congenital ichthyosis. Pediatr Dermatol. 2012.
Berg C, Geipl A, Kohl M et al. Prenatal sonographic features of harlequin ichthyosis. Arch Gynecol Obstet. 2003;268:48-51.
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