Related MeSH Hierarchy (4)
Diseases [C] » Nervous System Diseases [C10] » Cranial Nerve Diseases » Ocular Motility Disorders » Oculomotor Nerve Diseases » Congenital Cranial Dysinnervation Disorders
Diseases [C] » Nervous System Diseases [C10] » Nervous System Malformations » Congenital Cranial Dysinnervation Disorders
Diseases [C] » Eye Diseases [C11] » Ocular Motility Disorders » Oculomotor Nerve Diseases » Congenital Cranial Dysinnervation Disorders
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Nervous System Malformations » Congenital Cranial Dysinnervation Disorders
Description
Congenital neurodevelopmental diseases characterized by abnormal eye, eyelid, and facial movements. Congenital cranial dysinnervation disorders (CCDDs) are caused by abnormal innervation of CRANIAL NERVES (e.g., CNs III, IV and VI) resulting in aplasia or hypoplasia of the ocular and facial musculature involved in EYE MOVEMENTS. MeSH
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Subtype Terms (3)
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