References
- 1. Arikan II, Harma M, Barut A, Harma MI, Bayar U. Harlequin ichthyosis: a case report and review of literature. Anatolian Journal of Obstetrics and Gynecology. 2010;1:1-3.
- 2. Choate KA, Milstone LM. The ichthyoses. In: Kang S, Amagai M, Bruckner AL, Enk AH, Margolis DJ, Mc-Michael AJ, et al, editors. Fitzpatrick’s dermatology. 9th ed. New York: McGraw Hill Education; 2019. p. 775-815.
- 3. Scott CA, Rajpopat S, Di WL. Harlequin ichthyosis: ABCA12 mutations underlie defective lipid transport, reduced protease regulation and skin barrier dysfunction. Cell Tissue Res. 2013;351(2):281-8.10.1007/s00441-012-1474-922864982
- 4. Verma B, Abhinay A, Mohan A, Singh A. Congenital heart diseases in harlequin icthyosis - case series. J Family Med Prim Care. 2019;8(3):1266-8.10.4103/jfmpc.jfmpc_61_19648278731041289
- 5. Ahmed H, O’Toole EA. Recent advances in the genetics and management of harlequin ichthyosis. Pediatr Dermatol. 2014;31(5):539-46.10.1111/pde.1238324920541