Complex movement disorders in a sporadic Boucher-Neuhäuser Syndrome: Phenotypic manifestations beyond the triad

Movement Disorders

Volumn 24, Issue 15, 2009, Pages 2304-2306

  Ling, Helen ^a   Unnwongse, Kanjana ^b   Bhidayasiri, Roongroj ^a  

^a KING CHULALONGKORN MEMORIAL HOSPITAL   (Thailand)

^b Prasart Neurological Institute   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

LUTEINIZING HORMONE; TESTOSTERONE;

ADULT; BOUCHER NEUHAUSER SYNDROME; BRAIN ATROPHY; CASE REPORT; CEREBELLAR ATAXIA; CHOROID CAPILLARY LAYER; CHOROID DISEASE; GYNECOMASTIA; HUMAN; HYPOGONADOTROPIC HYPOGONADISM; LETTER; MALE; MOTOR DYSFUNCTION; NUCLEAR MAGNETIC RESONANCE IMAGING; OROMANDIBULAR DYSTONIA; PHENOTYPE; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RETINA MALFORMATION; SENSORIMOTOR NEUROPATHY; VISUAL IMPAIRMENT;

ENDOCRINE SYSTEM DISEASES; FAMILY HEALTH; FLUORESCEIN ANGIOGRAPHY; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; MOVEMENT DISORDERS; OCULAR MOTILITY DISORDERS; SPINOCEREBELLAR ATAXIAS;

EID: 72849134092     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.22831     Document Type: Letter

References (8)

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