Clinical and molecular spectrum of genetic hypertriglyceridaemia in North Indian children: a case series
Paediatric HTG is often detected incidentally. Genetic characterisation is crucial for prognosis because baseline TG levels are non-predictive. Drug therapy helps to reach treatment targets in most of the patients.
Authors
- Sayan Banerjee (ORCID: https://orcid.org/0000-0003-4191-3765)
- Savita Verma Attri (ORCID: https://orcid.org/0000-0002-1783-9094)
- Chennakeshava Thunga (ORCID: https://orcid.org/0000-0002-5346-7873)
- Inusha Panigrahi (ORCID: https://orcid.org/0000-0001-7375-9892)
- Arun George (ORCID: https://orcid.org/0009-0005-6601-8777)
- Jayakanthan Kabeerdoss (ORCID: https://orcid.org/0000-0002-7852-6657)
- Pamali Mahasweta Nanda (ORCID: https://orcid.org/0000-0001-8117-0658)
- Anju Bala (ORCID: https://orcid.org/0000-0001-9786-4347)
- Devi Dayal
- Sadhna Lal
Institutions
- Post Graduate Institute of Medical Education and Research (IN)
Publication Details
- Journal
- Pediatric Endocrinology Diabetes and Metabolism
- Published
- 2025-01-01
- DOI
- https://doi.org/10.5114/pedm.2025.148401
- Primary Topic
- Lipid metabolism and disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00