Filters
Term Search
You can select from the dropdown list OR enter your own terms to refine the search.
Last Updated: 10/31/2025
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 326 publications
Interesting Case of Familial Partial Lipodystrophy Syndrome (Type 6) with LIPE Gene Defect: A Case Report.
Journal: The Journal of the Association of Physicians of India
Published: June 24, 2025
Potential Impact of Parental Origin of Inheritance on the Clinical Presentation of Familial Partial Lipodystrophy Type 2 Syndrome.
Journal: Clinical endocrinology
Published: May 21, 2025
Diagnosis and Management of Genetic Lipodystrophy Syndromes and its Implications for Atherosclerosis.
Journal: Current atherosclerosis reports
Published: April 27, 2025
Heterozygous pathogenic PPARG variants in patients with severe hypertriglyceridemia.
Journal: Journal of clinical lipidology
Published: April 22, 2025
Calf skinfold measurements as a diagnostic tool for lipodystrophy syndromes: a cross-sectional study.
Journal: Diabetology & metabolic syndrome
Published: April 16, 2025
Brazilian expert consensus on the diagnosis, classification, screening for complications and treatment of familial partial lipodystrophy.
Journal: Diabetology & metabolic syndrome
Published: March 25, 2025
A case of familial partial lipodystrophy type 2 masquerading as Cushing syndrome: Explaining an atypical phenotype by whole-exome sequencing.
Journal: Archives of endocrinology and metabolism
Published: March 25, 2025
Novel and Ultra-Rare Heterozygous Mis-sense LMNA variants causing Familial Partial Lipodystrophy.
Journal: The Journal of clinical endocrinology and metabolism
Published: February 06, 2025
Genetics Evaluation Outcomes From an Academic Multidisciplinary Atypical Diabetes Program.
Journal: Journal of the Endocrine Society
Published: January 28, 2025
Tirzepatide for Lipodystrophy.
Journal: medRxiv : the preprint server for health sciences
Published: January 13, 2025
"I suffer from several serious diseases." Dunnigan type of familial partial lipodystrophy: a multiple-symptom disorder caused by a genetic mutation.
Journal: Polish archives of internal medicine
Published: January 07, 2025
Last Updated: 10/31/2025