Recurrent Congenital Ichthyosis in Newborn: A Case Report
Keywords:
Autosomal Recessive, Congenital ichthyosis, Skin lesion
Abstract
Ichthyosis refers to a relatively uncommon group of skin disorders characterized by the presence of excessive amounts of dry surface scales. It can be congenital or acquired. Our patient was third child with this disorder and out of three none survived. In congenital ichthyosis form of disorders, routine histopathology, electron microscopy, and frozen sections of skin biopsy specimens may be required to determine the specific classification of disease. The mainstay of therapy includes removal of surface scales and application of a water barrier. In disabling cases, oral retinoids may reduce cosmetic disfigurement, depression, and social isolation.
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References
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2. Okulicz JF, Schwartz RA. Hereditary and acquired ichthyosis vulgaris. International Journal of Dermatology 2003;42(2): 95-8. [PubMed]
3. Thappa DM, Clinical Pediatric Dermatology 2009:1:121.
4. Moeschler JB, Shevell M. Clinical genetic evaluation of the child with mental retardation or developmental delays. Pediatrics 2006;117(6):2304-16. [PubMed]
5. Dhar S, Color Atlas and Synopses of Pediatric Dermatology 2008:2:32-33.
6. Scheinfeld N, Libkind M, Freilich S. New-onset ichthyosis and diabetes in a 14-year-old Pediatric dermatology 2001;18(6):501–3. [PubMed]
7. 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.
CITATION
DOI: 10.17511/ijmrr.2013.i02.05
Published: 2013-06-30
How to Cite
1.
Patil P, Patil A, Verma J, Ghosh G. Recurrent Congenital Ichthyosis in Newborn: A Case Report. Int J Med Res Rev [Internet]. 2013Jun.30 [cited 2024Dec.23];1(2):71-3. Available from: https://ijmrr.medresearch.in/index.php/ijmrr/article/view/11
Section
Case Report
OAI - Open Archives Initiative
