Case report of harlequin ichthyosis who had similar history in two earlier siblings

Authors

  • Shazia Rasul
  • Asma Gul
  • Shabnum Tahir
  • Abdul Hameed

References

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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Published

2016-12-02

How to Cite

1.
Rasul S, Gul A, Tahir S, Hameed A. Case report of harlequin ichthyosis who had similar history in two earlier siblings. J Pak Assoc Dermatol [Internet]. 2016Dec.2 [cited 2025Mar.15];24(4):369-70. Available from: http://jpad.com.pk/index.php/jpad/article/view/232

Issue

Vol. 24 No. 4 (2014): October - December

Section

Short Communications

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