Catalog
Bannayan-Riley-Ruvalcaba syndrome
No MMS code
Link to WHO Definition
Bannayan-Riley-Ruvalcaba syndrome – http://id.who.int/icd/entity/357383447
Bannayan-Riley-Ruvalcaba syndrome is characterised by an abnormally large head (macrocephaly), multiple hamartomatous polyps in the intestines, benign tumours of fatty tissues just below the skin, and excessive growth before and after birth.
Parents
- LD2D Phakomatoses or hamartoneoplastic syndromes
- EC23.1 Syndromic genetically-determined hypermelanosis or lentiginosis
- LD27.5 Genetic hamartoneoplastic syndromes affecting the skin
- Inherited cancer-predisposing syndromes
- Syndromic conditions with disorders of intellectual development as a relevant clinical feature
- PTEN Hamartoma tumour syndrome