International Journal of Health & Allied Sciences

CASE REPORT
Year
: 2013  |  Volume : 2  |  Issue : 3  |  Page : 203--205

Hypomelanosis of Ito: A rare cutaneous syndrome


Hari Kishan Yadalla Kumar, Sushmitha Jayaprasad 
 Department of Dermatology, MVJ Medical College and Research Hospital, Hoskote, Bangalore, India

Correspondence Address:
Hari Kishan Yadalla Kumar
Department of Dermatology, Res: 70, Padma Nivasa, Skin Care Clinic, 3rd Cross MG Extension, HV Halli, Raja Rajeswari Nagar, Bangalore 560 098
India

Hypomelanosis of Ito, also known as Incontinentia Pigmenti Achromians of Ito (IPA), is a rare cutaneous syndrome clinically characterized by macular hypopigmented whorls, patches, and streaks either unilateral or bilateral following lines of Blaschko. These skin lesions become apparent at birth or during childhood and normally are present on the trunk, occasionally on the extremities, and rarely on the face. Most patients have multisystem involvement and may show chromosomal mosaicism, the most common being neurological, muscular, skeletal, and ocular. We present a male child of 5-years-old with hypopigmented whorls and patches along the lines of Blaschko present on both sides of the trunk since birth. The child had no other systemic abnormality. The importance of this cutaneous condition and its association with other system involvement has been emphasized in this article.


How to cite this article:
Kumar HY, Jayaprasad S. Hypomelanosis of Ito: A rare cutaneous syndrome .Int J Health Allied Sci 2013;2:203-205


How to cite this URL:
Kumar HY, Jayaprasad S. Hypomelanosis of Ito: A rare cutaneous syndrome . Int J Health Allied Sci [serial online] 2013 [cited 2021 Oct 19 ];2:203-205
Available from: https://www.ijhas.in/article.asp?issn=2278-344X;year=2013;volume=2;issue=3;spage=203;epage=205;aulast=Kumar;type=0