ORPHA:2526
Microcephaly-chorioretinopathy-lymphedema syndrome
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:2526 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Microcephaly
- Abnormality of the eye
- Abnormality of vision
- Lymphedema
- Myopia
- Edema