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AKT2-related familial partial lipodystrophy

ORPHA: 79085

Contents

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

Overview

human disease

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 AKT2-related familial partial lipodystrophy, sourced from HPO and Orphanet clinical annotations.

Insulin resistanceLipodystrophyAcanthosis nigricansHepatic steatosisHypertriglyceridemiaHepatomegalyDecreased serum leptinIncreased intraabdominal fatDecreased adiponectin levelPolycystic ovariesInsulin-resistant diabetes mellitusOligomenorrhea

Classification & Codes

Orphanet Code

ORPHA:79085
AKT2-related familial partial lipodystrophy
OrphanetORPHA:79085
Treatments0 drug(s)
Symptoms on record12 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO