Encephalocraniocutaneous lipomatosis (Q90781): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/1084215843 / rank | |||
Normal rank | |||
Revision as of 17:46, 15 August 2026
Encephalocraniocutaneous lipomatosis is a rare sporadic neurocutaneous syndrome involving tissues of ectodermal and mesodermal origin and characterised by profound mental retardation, early onset of seizures, unilateral temporofrontal lipomatosis, ipsilateral cerebral and leptomeningeal lipomatosis, cerebral malformation and calcification, and lipomas of the skull, eye, and heart.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1084215843 |
||
| English | Encephalocraniocutaneous lipomatosis |
Encephalocraniocutaneous lipomatosis is a rare sporadic neurocutaneous syndrome involving tissues of ectodermal and mesodermal origin and characterised by profound mental retardation, early onset of seizures, unilateral temporofrontal lipomatosis, ipsilateral cerebral and leptomeningeal lipomatosis, cerebral malformation and calcification, and lipomas of the skull, eye, and heart. |
