Dyskinesias. Abnormal Movements . Hemiballism . Linguofacial Dyskinesia . Oral Dyskinesia . Oral-Facial Dyskinesia . Tardive Oral Dyskinesia . Abnormal Movement . Dyskinesia . Dyskinesia, Lingual-Facial-Buccal . Dyskinesia, Linguofacial . Dyskinesia, Oral . Dyskinesia, Oral-Facial . Dyskinesia, Orofacial . Dyskinesias, Lingual-Facial-Buccal . Dyskinesias, Linguofacial . Dyskinesias, Oral . Dyskinesias, Oral-Facial . Dyskinesias, Orofacial . Involuntary Movement . Lingual Facial Buccal Dyskinesia . Lingual-Facial-Buccal Dyskinesias . Linguofacial Dyskinesias . Movement, Abnormal . Movement, Involuntary . Movements, Abnormal . Movements, Involuntary . Oral Dyskinesias . Oral Facial Dyskinesia . Oral-Facial Dyskinesias . Orofacial Dyskinesias . Tardive Oral Dyskinesias . Asterixis . Ballismus . Hemiballismus . Involuntary Movements . Lingual-Facial-Buccal Dyskinesia . Orofacial Dyskinesia . DYSKINESIA . Abnormal involuntary movements which primarily affect the extremities, trunk, or jaw that occur as a manifestation of an underlying disease process. Conditions which feature recurrent or persistent episodes of dyskinesia as a primary manifestation of disease may be referred to as dyskinesia syndromes (see MOVEMENT DISORDERS). Dyskinesias are also a relatively common manifestation of BASAL GANGLIA DISEASES. . 1.00
Orofaciodigital Syndromes. Dysplasia Linguofacialis . Oral-Facial-Digital Syndrome . Oral-Facial-Digital Syndrome, Type I . Oral-Facial-Digital Syndrome, Type II . Oro-Facio-Digital Syndrome . Orodigitofacial Dysostosis . Orodigitofacial Syndrome . Orofaciodigital Syndrome . Orofaciodigital Syndrome I . Orofaciodigital Syndrome II . Gorlin Psaume Syndrome . Oral Facial Digital Syndrome, Type I . Oral Facial Digital Syndrome, Type II . Orofaciodigital Syndrome IIs . Orofaciodigital Syndrome Is . Papillon Leage and Psaume Syndrome . Syndrome, Gorlin-Psaume . Syndrome, Mohr . Syndrome, Orofaciodigital . Syndromes, Orofaciodigital . Gorlin-Psaume Syndrome . Mohr Syndrome . Papillon-Leage and Psaume Syndrome . Two syndromes of oral, facial, and digital malformations. Type I (Papillon-Leage and Psaume syndrome, Gorlin-Psaume syndrome) is inherited as an X-linked dominant trait and is found only in females and XXY males. Type II (Mohr syndrome) is inherited as an autosomal recessive trait. . 0.71
