Related MeSH Hierarchy (6)
Diseases [C] » Nervous System Diseases [C10] » Cranial Nerve Diseases » Ocular Motility Disorders » Oculomotor Nerve Diseases » Congenital Cranial Dysinnervation Disorders » Mobius Syndrome
Diseases [C] » Eye Diseases [C11] » Ocular Motility Disorders » Oculomotor Nerve Diseases » Congenital Cranial Dysinnervation Disorders » Mobius Syndrome
Diseases [C] » Stomatognathic Diseases [C07] » Mouth Diseases » Facial Nerve Diseases » Mobius Syndrome
Diseases [C] » Nervous System Diseases [C10] » Cranial Nerve Diseases » Facial Nerve Diseases » Mobius Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Abnormalities, Multiple » Mobius Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Infant, Newborn, Diseases » Mobius Syndrome
Description
A syndrome of congenital facial paralysis, frequently associated with abducens palsy and other congenital abnormalities including lingual palsy, clubfeet, brachial disorders, cognitive deficits, and pectoral muscle defects. Pathologic findings are variable and include brain stem nuclear aplasia, facial nerve aplasia, and facial muscle aplasia, consistent with a multifactorial etiology. (Adams et al., Principles of Neurology, 6th ed, p1020) MeSH
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