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.

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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
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article

Interesting Case of Familial Partial Lipodystrophy Syndrome (Type 6) with LIPE Gene Defect: A Case Report

V. Damle, Viswanathan Mohan, R. Lavanya, K Vijayalakshmi et al.
1 citations
Journal of the Association of Physicians of India
Nuclear Structure and Function
0.81
article

Interesting Case of Familial Partial Lipodystrophy Syndrome (Type 6) with LIPE Gene Defect: A Case Report

V. Damle, Viswanathan Mohan, R. Lavanya, K Vijayalakshmi, Akshay Patil, Venkatesan Radha, A. Regina
article en
1 citations

Abstract

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.

Journal of the Association of Physicians of IndiaVol. 73(5)
Madras Diabetes Research Foundation (IN), Dr. Mohan's Diabetes Specialities Centre (IN)
Good health and well-being
Openalex Percentile: Top 27%
Nuclear Structure and Function
0.81
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Interesting Case of Familial Partial Lipodystrophy Syndrome (Type 6) with LIPE Gene Defect: A Case Report — V. Damle, Viswanathan Mohan, et al. · Journal of the Association of Physicians of India (2025) | TGRS Research Map | TGRS