Interesting Case of Familial Partial Lipodystrophy Syndrome (Type 6) with LIPE Gene Defect: A Case Report
We report on an interesting case of familial partial lipodystrophy syndrome (type 6) due to a LIPE gene defect. Lipodystrophy syndromes are characterized by dysfunctional adipose tissue. While there are several types of lipodystrophies, this report is of a case of familial partial lipodystrophy with a LIPE gene mutation, which is very rare. Because the LIPE gene defect was of heterozygous nature, it presented in a milder clinical form. Thanks to genetic testing, we were able to clinch the diagnosis in this case. This case teaches us that we should have a high index of suspicion to pick up such rare cases and to offer genetic testing whenever indicated.
Authors
- V. Damle
- Viswanathan Mohan (ORCID: https://orcid.org/0000-0001-5038-6210)
- R. Lavanya
- K Vijayalakshmi
- Akshay Patil
- Venkatesan Radha (ORCID: https://orcid.org/0000-0002-4281-0250)
- A. Regina
Institutions
- Madras Diabetes Research Foundation (IN)
- Dr. Mohan's Diabetes Specialities Centre (IN)
Publication Details
- Journal
- Journal of the Association of Physicians of India
- Published
- 2025-01-01
- DOI
- https://doi.org/10.59556/japi.73.0932
- Citations
- 1
- Primary Topic
- Nuclear Structure and Function
- Type
- article
- Field-Weighted Citation Impact
- 0.81