ORPHA:1296
Lambert syndrome
Also called Branchial dysplasia-intellectual disability-inguinal hernia syndrome
- Body system
- Neurological diseases
- Inheritance pattern
- Unknown
- Typical age of onset
- Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:1296 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Inguinal hernia
- Wide mouth
- Malar flattening
- Intellectual disability
- Intrauterine growth retardation
- Failure to thrive in infancy