Search for a rare disease
Other search option(s)
Noonan syndrome with multiple lentigines
Disease definition
A rare multisystem genetic disorder characterized by lentigines, hypertrophic cardiomyopathy, short stature, pectus deformity, and dysmorphic facial features.
ORPHA:500
Classification level: DisorderDetailed information
Article for general public
Professionals
- Review article
- English (2008)
- Clinical practice guidelines
- Français (2016, pdf)
- Clinical genetics review
- English (2015)
Additional information
Further information on this disease
Health care resources for this disease
Research activities on this disease
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.