Familial Partial Lipodystrophy Kobberling Type C1720859
A rare inherited disorder where fat is lost from the arms and legs but accumulates around the face and trunk. It can lead to metabolic complications like diabetes and high triglycerides. Management focuses on treating metabolic abnormalities and monitoring complications.
Key facts at a glance
- ICD-10
- E88.9
- ICD-11
- 5A00.0
- Body system
- metabolic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Fatigue or weight changes
(metabolic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Loss of subcutaneous fat in limbs
(metabolic)Insulin resistance
(metabolic)Hypertriglyceridemia
(metabolic)Hepatomegaly
(metabolic)Medication Comparisons
Compare medications used to treat Familial Partial Lipodystrophy Kobberling Type C1720859. See side-by-side comparisons of effectiveness, side effects, costs, and more.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy