Berardinelli–Seip congenital lipodystrophy type-2: a case series of three Indian children
CGL is a rare but distinct disorder that should be considered in children presenting with generalised muscularity, hepatomegaly, and metabolic abnormalities.
Authors
- Swati Dokania
- Anuradha Rai (ORCID: https://orcid.org/0000-0002-5402-6076)
- Surbhi Gyani
- Seema Kapoor
- Prabhakar Bindhu
- Mithila Das Mazumder
- Medha Mittal
Institutions
- Pacific Dental College and Hospital (IN)
- Pacific Medical (China) (CN)
- Chacha Nehru Bal Chikitsalaya (IN)
- All India Institute of Medical Sciences (IN)
Publication Details
- Journal
- Journal of Pediatric Endocrinology and Metabolism
- Published
- 2026-01-30
- DOI
- https://doi.org/10.1515/jpem-2025-0514
- Primary Topic
- Nuclear Structure and Function
- Type
- article
- Field-Weighted Citation Impact
- 0.00