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PMID: 11223857 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Behavior phenotype in the RSH/Smith-Lemli-Opitz syndrome.

American journal of medical genetics ·Vol. 98 ·No. 2 ·2001-01-15 ·Pages 191-200

Tierney E, Nwokoro NA, Porter FD, Freund LS, Ghuman JK, Kelley RI

Abstract

The behavior phenotype of Smith-Lemli-Opitz syndrome (SLOS) was studied by assessing behavior, social, and communication abilities, sensory hyperreactivity, and the deficits associated with autistic disorder. Fifty-six SLOS subjects, age 0.3 to 32.3 years, were evaluated by multiple age-dependent questionnaires and telephone interviews. Of the 56 subjects, 50 (89%) had a history of repeated self-injury: 30 (54%) bit themselves; 27 (48%) head-banged; and 30 (54%) threw themselves backward in a highly characteristic upper body movement ("opisthokinesis"). Forty-seven of these subjects were also evaluated by direct observation and by direct interview of the parent or caregiver. Of 11 subjects 10 years or older, three (27%) had a stereotypic stretching motion of the upper body accompanied by hand flicking. Additional measures showed sensory hyperreactivity, temperament dysregulation, sleep disturbance, and social and communication deficits. Nine of 17 subjects (53%) met the diagnostic criteria for autistic disorder by the Autism Diagnostic Interview-Revised (ADI-R) algorithm questions [Lord et al., 1993, 1994]. Thus, SLOS is a metabolic disorder that can be associated with autism and other behavioral characteristics that define a distinctive and diagnostically important behavioral disorder.

MeSH Terms
Adolescent Adult Algorithms Autistic Disorder/complications,diagnosis Behavior Child Child, Preschool Cholesterol/therapeutic use Female Humans Infant Interpersonal Relations Interview, Psychological Male Motor Activity Phenotype Sensation Disorders/complications Smith-Lemli-Opitz Syndrome/genetics,physiopathology,psychology
Chemicals
Cholesterol
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Tierney E
Department of Psychiatry, Kennedy Krieger Institute, Baltimore, Maryland 21231, USA. tierney@kennedykrieger.org
Nwokoro N A
Porter F D
Freund L S
Ghuman J K
Kelley R I
Article Info
Journal
American journal of medical genetics
Abbr.
Am J Med Genet
ISSN
0148-7299
Published
2001-01-15
Pages
191-200
Language
English
Region
United States
NLM ID
7708900
Subset
IM
Grants
NIMH NIH HHS · K23 MH001883-01A1 · United States
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