First diagnosis of familial partial lipodystrophy syndrome type 3 during pregnancy associated with a novel heterozygous PPARG variant and a concurrent ABCC8 variant: a case report.
- DOI
- 10.3389/fendo.2026.1855679
- Published
- 2026
- Container
- Frontiers in endocrinology
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.3389/fendo.2026.1855679,
title = {First diagnosis of familial partial lipodystrophy syndrome type 3 during pregnancy associated with a novel heterozygous PPARG variant and a concurrent ABCC8 variant: a case report.},
author = {Holstein A and Jabri I and Linck JA and Tönjes A and Holstein DJF and Kovacs P and Pirlich L},
year = {2026},
journal = {Frontiers in endocrinology},
doi = {10.3389/fendo.2026.1855679},
url = {https://doi.org/10.3389/fendo.2026.1855679}
}RIS
TY - JOUR TI - First diagnosis of familial partial lipodystrophy syndrome type 3 during pregnancy associated with a novel heterozygous PPARG variant and a concurrent ABCC8 variant: a case report. AU - Holstein A AU - Jabri I AU - Linck JA AU - Tönjes A AU - Holstein DJF AU - Kovacs P AU - Pirlich L PY - 2026 JO - Frontiers in endocrinology DO - 10.3389/fendo.2026.1855679 UR - https://doi.org/10.3389/fendo.2026.1855679 ER -
APA
A, H., I, J., JA, L., A, T., DJF, H., P, K., & L, P. (2026). First diagnosis of familial partial lipodystrophy syndrome type 3 during pregnancy associated with a novel heterozygous PPARG variant and a concurrent ABCC8 variant: a case report.. Frontiers in endocrinology. https://doi.org/10.3389/fendo.2026.1855679
Source records
- pubmed · retrieved 2026-09-26T11:05:46.572Z