Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Smith-Magenis syndrome: case report and review].

Archivos argentinos de pediatria - 1 Apr 2008

Bronberg Rubén, Ziembar María, Drut Mónica, Goldschmidt Ernesto

Abstract excerpt

Smith-Magenis syndrome (SMS) is characterized by distinctive facial features that progress with age, developmental delay, cognitive impairment, and behavioral abnormalities associated with molecular anomaly in 17p11.2. Treatment includes: early childhood intervention programs, special education, vocational training later in life, and speech/language, physical, and occupational, behavioral, and sensory integration...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Cognition Disorders
Share to Developmental Disabilities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Karyotyping

Share to Mental Disorders

Share to Phenotype

Share to Syndrome

Source

Identifiers

PMID: 18661040
DOI: 10.1590/S0325-00752008000200009

Genes

SMS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Smith-Magenis syndrome: case report and review].PMID 18661040Read ↗

[Smith-Magenis syndrome: a report of two new cases and an approximation to their characteristic behavioural phenotype].Semantic proximity Read ↗

A Turkish patient with large 17p11.2 deletion presenting with Smith Magenis syndrome.Semantic proximity Read ↗

Behavioral phenotype of Smith-Magenis syndrome (del 17p11.2).Semantic proximity Read ↗

A case report of monozygotic twins with Smith-Magenis syndrome.Semantic proximity Read ↗

[Clinical characteristics and genetic analysis of a neonate with Smith-Magenis syndrome].Semantic proximity Read ↗

Smith-Magenis Syndrome—Clinical Review, Biological Background and Related DisordersSemantic proximity Read ↗

Smith-Magenis Syndrome: Face Speaks.Semantic proximity Read ↗

Smith-Magenis syndrome: Clinical and behavioral characteristics in a large retrospective cohort.Semantic proximity Read ↗

Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 cases.Semantic proximity Read ↗

Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)Semantic proximity Read ↗

First Case Report of Smith-Magenis Syndrome (SMS) Among the Arab Community in Nazareth: View and Overview.Semantic proximity Read ↗

[Diagnostic difficulties in Smith-Magenis Syndrome (SMS) on the basis of own experience and literature data].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.