ORPHA:2398
Multiple symmetric lipomatosis
Also called Cephalothoracic lipodystrophy, Familial benign cervical lipomatosis, Launois-Bensaude lipomatosis, Madelung disease
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal dominant, Autosomal recessive, Mitochondrial inheritance, Not applicable
- Typical age of onset
- Adolescent, Adult, Childhood, Elderly
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:2398 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Multiple lipomas
- Joint stiffness
- Arthralgia
- Abnormal adipose tissue morphology
- Insulin resistance
- Gait disturbance