Congenital cranial dysinnervation syndrome (Q41905): 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/691350959 / rank
 
Normal rank

Revision as of 08:13, 13 August 2026

Congenital cranial dysinnervation syndrome is a group of congenital cranial dysinnervation disorders (CCDDs). CCDDs are congenital, non-progressive conditions that result from abnormal development of the cranial nerves and their nuclei. They include both sporadic and familial disorders, and since they frequently involve the extraocular and facial musculature and result in abnormal eye movements, they often present to the ophthalmologist.
Language Label Description Also known as
default for all languages
9C82.2
    English
    Congenital cranial dysinnervation syndrome
    Congenital cranial dysinnervation syndrome is a group of congenital cranial dysinnervation disorders (CCDDs). CCDDs are congenital, non-progressive conditions that result from abnormal development of the cranial nerves and their nuclei. They include both sporadic and familial disorders, and since they frequently involve the extraocular and facial musculature and result in abnormal eye movements, they often present to the ophthalmologist.

      Statements