familial partial lipodystrophy type 1

ORPHA: 79084

Contents

1. Overview
2. Available Treatments
3. Clinical Presentation
4. Classification & Codes

Overview

familial partial lipodystrophy characterized by loss of adipose tissue that is confined to the extremities with normal or increased fat in other areas of the body

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with familial partial lipodystrophy type 1, sourced from HPO and Orphanet clinical annotations.

Polycystic ovariesDiabetes mellitusHypertensionHyperinsulinemiaInsulin resistanceAcanthosis nigricansXanthomatosisHepatic steatosisCoronary artery atherosclerosisPancreatitisHepatomegalyLipoatrophy

Classification & Codes

Orphanet Code

ORPHA:79084

familial partial lipodystrophy type 1

Orphanet	`ORPHA:79084`
Treatments	0 drug(s)
Symptoms on record	12 signs
Status	published

Factual Authority

Last Updated3/20/2026

Clinical DataHPO · Orphanet

Drug DataFDA · EMA · CDSCO