Neurologic and Developmental Features of the Smith-Magenis Syndrome (del 17p11.2)

Pediatric Neurology

Volumn 34, Issue 5, 2006, Pages 337-350

  Gropman, Andrea L ^a,b   Duncan, Wallace C ^c   Smith, Ann C M ^a,b  

^a GEORGETOWN UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^c NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACEBUTOLOL; ANTICONVULSIVE AGENT; ATOMOXETINE; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; CENTRAL STIMULANT AGENT; FLUOXETINE; LITHIUM; MELATONIN; MOOD STABILIZER; NEUROLEPTIC AGENT; RISPERIDONE; SEROTONIN UPTAKE INHIBITOR; VALPROIC ACID;

ACTIMETRY; AUTOMUTILATION; AWARENESS; BEHAVIOR CHANGE; BITE; BODY WEIGHT DISORDER; BRACHYCEPHALY; BRACHYDACTYLY; CENTRAL NERVOUS SYSTEM; CHILDHOOD; CHROMOSOME 17P; CIRCADIAN RHYTHM; CLINICAL FEATURE; CLINICAL TRIAL; COGNITION; CYTOGENETICS; DEMOGRAPHY; DIAGNOSTIC PROCEDURE; DOWN SYNDROME; EYE DISEASE; FACIES; FAMILY; GENE DELETION; HOARSENESS; HUMAN; HYPERACTIVITY; INFANCY; INFANTILE HYPOTONIA; LANGUAGE DISABILITY; LARYNX DISORDER; LETHARGY; MENTAL DEFICIENCY; METHODOLOGY; NERVOUS SYSTEM DEVELOPMENT; ONYCHOTILLOMANIA; PERIPHERAL NERVOUS SYSTEM; PHENOTYPE; POLYEMBOLOKOILAMANIA; POLYSOMNOGRAPHY; PRIORITY JOURNAL; PROGNATHIA; PSYCHOMOTOR RETARDATION; PSYCHOSIS; REVIEW; SKELETON MALFORMATION; SLEEP DISORDER; SMITH MAGENIS SYNDROME; SPEECH DISORDER; WEIGHT GAIN;

ABNORMALITIES, MULTIPLE; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 17; HUMANS; MENTAL RETARDATION; SYNDROME;

EID: 33646125422     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2005.08.018     Document Type: Review

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