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Griscelli Syndrome in Two Siblings with Silvery Hair: A Case Report
Hanniyah Khwaja1, A R Rajan2, Nitin Lingayat2
1Symbiosis Medical College for Women & Symbiosis University Hospital & Research Centre, Symbiosis International (Deemed University), Pune, India.
JNMA; Journal of the Nepal Medical Association
|March 5, 2026
Summary
Griscelli syndrome (GS) is a rare disorder causing partial albinism and immune/neurological issues. Early diagnosis in neonates is crucial for timely treatment like bone marrow transplant to prevent severe complications.
Area of Science:
- Genetics and Immunology
- Pediatric Rare Diseases
Background:
- Griscelli syndrome (GS) is a rare genetic disorder.
- It presents with partial albinism, immune deficiency, and neurological impairment.
- Three variants (GS1, GS2, GS3) exhibit diverse phenotypes.
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