Indian Dermatology Online Journal

CASE REPORT
Year
: 2016  |  Volume : 7  |  Issue : 6  |  Page : 506--508

Griscelli syndrome type-3


Bela J Shah, Ashish K Jagati, Nilesh K Katrodiya, Sonal M Patel 
 Department of Dermatology, BJ Medical College and Civil Hospital, Ahmedabad, Gujarat, India

Correspondence Address:
Bela J Shah
1st Floor, Room No. 139, Wing No. 3, OPD Building, Civil Hospital, Asarwa, Ahmedabad, Gujarat
India

Griscelli syndrome (GS) is a rare autosomal recessive multisystem disorder of pigmentary dilution of skin, silver gray hair, variable immunodeficiency, neurological impairment, and abnormal accumulation of melanosomes in melanocytes. GS type 3 is characterized by hypomelanosis with no immunological and neurological manifestation. Prognosis is very good in type 3 GS and usually require no active intervention, as opposed to type 1 and 2 where early diagnosis and treatment plays a crucial role in patient's survival. The characteristic phenotypic appearance, especially the pigment dilution of the patient's hair, is emphasized here.


How to cite this article:
Shah BJ, Jagati AK, Katrodiya NK, Patel SM. Griscelli syndrome type-3.Indian Dermatol Online J 2016;7:506-508


How to cite this URL:
Shah BJ, Jagati AK, Katrodiya NK, Patel SM. Griscelli syndrome type-3. Indian Dermatol Online J [serial online] 2016 [cited 2019 Jun 25 ];7:506-508
Available from: http://www.idoj.in/article.asp?issn=2229-5178;year=2016;volume=7;issue=6;spage=506;epage=508;aulast=Shah;type=0