Year: 2025
Type: article
Study design: Case Report
Abstract: Griscelli syndrome is a rare autosomal recessive disorder characterized by pigmentary dilution of the skin and hair, associated with various systemic manifestations resulting from underlying genetic mutations. We report the case of a 5-year-old girl with no significant medical history who was admitted to the pediatric department for evaluation of hemophagocytic lymphohistiocytosis. She was noted to have gray hair, eyelashes,and eyebrows since birth. Trichoscopic examination revealed hypopigmented hair shafts lacking pigment clumps but displaying regularly spaced pigment clusters arranged in a discontinuous linear pattern, findings consistent with Griscelli syndrome.
Language: English
Subfield: Dermatology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
OpenAlex ID: W7123347356