Benign Paroxysmal Torticollis of Infancy

Benign Paroxysmal Torticollis of Infancy(来自ICD-11)

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Benign Paroxysmal Torticollis of Infancy is related to torticollis and migraine with or without aura 1. An important gene associated with Benign Paroxysmal Torticollis of Infancy is CACNA1A (Calcium Voltage-Gated Channel Subunit Alpha1 A). Related phenotypes are torticollis and ataxia

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