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

Authors

  • Shazia Rasul Departments of Obstetrics & Gynecology, Shalamar Medical & Dental College Lahore
  • Asma Gul Departments of Obstetrics & Gynecology, Shalamar Medical & Dental College Lahore
  • Shabnum Tahir Departments of Obstetrics & Gynecology, Shalamar Medical & Dental College Lahore
  • Abdul Hameed Consultant Dermatologist, Defence Skin & Laser Center, Lahore

DOI:

https://doi.org/10.66344/jpad.v24i4.232

References

1. Rodriguez-Pazos L, Ginarte M, Vega A et al. Autosomal recessive congenital ichthyosis. Actas Dermosifilioger. 2013;104:270-84.

2. Murphy-Brown L, Vella JA, Lawlor-Klean P. Harlequin ichthyosis: a case study. Neonatal Netw. 2004;23:7-12.

3. Akiyama, M. The pathogenesis of severe congenital ichthyosis of the neonate. J Dermatol Sci. 1999;21:96-104.

4. Habib A, Pasha W, Raza N et al. Harlequin ichthyosis in two siblings. J Coll Physicians Surg Pak. 2011:21:505-5.

5. Peterson H, Lofgren S, Bremmer S, Krol A. Novel ABCA-12 mutations leading to recessive congenital ichthyosis. Pediatr Dermatol. 2012.

6. 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

02.12.2016

Issue

Section

Short Communications

How to Cite

1.
Case report of harlequin ichthyosis who had similar history in two earlier siblings. J Pak Assoc Dermatol [Internet]. 2016 Dec. 2 [cited 2026 Aug. 6];24(4):369-70. Available from: https://www.jpad.com.pk/index.php/jpad/article/view/232