
Living with Congenital generalized lipodystrophy type 3
A rare inherited condition with very little body fat, extreme insulin resistance and early diabetes.
Understanding Congenital generalized lipodystrophy type 3
It is marked by very little fat tissue, extreme insulin resistance, high blood fats (triglycerides), a fatty liver and diabetes that starts early.
Signs & symptoms
GARD doesn't list a separate symptom list for this type. The summary describes:
- Very little body fat
- Extreme insulin resistance
- High triglycerides
- Fatty liver (hepatic steatosis)
- Early-onset diabetes
Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.
Diagnosis
- 1Talk with your doctor
Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.
- 2See a specialist
Your doctor may refer you to a specialist who knows rare conditions.
- 3Ask which tests can help
Your care team will decide which exams and tests can confirm the diagnosis.
Care & treatment
- Care team
- A doctor familiar with rare conditions, plus specialists as needed
- Expert care
- Ask about multidisciplinary care centers for rare conditions
- Treatment
- GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
- Research
- Clinical trials and observational studies may be options. See the research section below.
General information, not medical advice. Your care team makes the decisions.
Everyday life
Living with a rare condition is easier with support.
- Connect with Lipodystrophy United
- Keep notes on symptoms, changes and questions for appointments
- Ask about patient registries that help research
- Look into financial aid and travel resources for care visits
Quick facts
GARD doesn't name a gene here. It is autosomal recessive, so a child inherits a changed copy of the gene from each parent.
Also known as: berardinelli-seip congenital lipodystrophy type 3; berardinelli-seip congenital lipodystrophy, type 3; bscl3; cav1 congenital generalised lipodystrophy (disease); cav1 congenital generalized lipodystrophy (disease); cgl3
Patient organizations
- Lipodystrophy UnitedCongenital generalized lipodystrophy type 3 · United States
You are more than your diagnosis
Perspectives from people navigating life with Congenital generalized lipodystrophy type 3.
Explore research for Congenital generalized lipodystrophy type 3
Explore actively recruiting Congenital generalized lipodystrophy type 3 studies with HealthSpark.
Find actively recruiting studies for Congenital generalized lipodystrophy type 3 with HealthSpark. Share your city to explore research near you.
- Recruiting studies from ClinicalTrials.gov
- Share your city to look for research near you
- Eligibility is confirmed by the study team
Powered by HealthSpark, our AI chat helper
I can help you find recruiting Congenital generalized lipodystrophy type 3 studies. Enter a ZIP code, address or city below and I'll look within 50 miles.
Powered by HealthSpark, our AI chat helper · Study information from ClinicalTrials.gov · Eligibility is confirmed by the study team.
Get Signals for Congenital generalized lipodystrophy type 3
Stay in the loop with community stories and updates from medical researchers.
Create a living journal that talks back
HealthStory evolves private journaling with a living AI journal that talks back and asks thoughtful questions, helping you capture your Congenital generalized lipodystrophy type 3 experiences more deeply and prepare for better conversations with your doctors and care team.
Your journal is private. Sharing your story publicly is a separate choice, made with Share your story above.



