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Article

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

Medicine - 1 Jan 2016

Nijim Yousif, Adawi Amin, Bisharat Bishara, Bowirrat Abdalla

Abstract excerpt

Smith-Magenis syndrome (SMS0) is a complex and rare genetic multisystem disorder characterized by a variable pattern of cognitive deficits accompanied by a1 distinctive behavioral phenotype. SMS is characterized by subtle facial dysmorphology, short stature, sleep disturbances, and neurobehavioral abnormalities. Little is known about the manifestation of his unique case among Arab population and its strategic...

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Source

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Identifiers

PMID: 26817868
DOI: 10.1097/MD.0000000000002362
PMCID: PMC4998242

Genes

SMS
RAI1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

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