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Updated: Jun 5, 2026

Single Myofiber Isolation and Culture from a Murine Model of Emery-Dreifuss Muscular Dystrophy in Early Post-Natal Development
Published on: July 1, 2020
Idiopathic myelofibrosis in an infant
Rupali R Bavikar1, Rajesh K Kulkarni, Ashok D Rathod
1Department of Pathology, Lilavati Hospital and Research Centre, Bandra (W), Mumbai, India.
Abstract:
Idiopathic Myelofibrosis (MF) is an extremely rare condition in children. It has a very variable clinical spectrum. Cases of secondary myelofibrosis associated with Vitamin D deficiency and Systemic Lupus Erythematosus have been reported from India .In this case report, the authors describe clinical signs, laboratory findings and histologic features in a 6 month old infant with Idiopathic myelofibrosis.
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