Clinical, cognitive, behavioral and communicative features of Smith-Magenis Syndrome
Características clínicas, comportamentais, cognitivas e comunicativa na Síndrome Smith-Magenis
Dionísia Aparecida Cusin Lamônica; Greyce Kelly da Silva; Renata Heloísa Furlan; Dagma Venturini Marques Abramides; Gustavo Henrique Vieira; Danilo Moretti-Ferreira; Célia Maria Giacheti
Abstract
Background: this study aimed to describe the clinical, behavioral, cognitive and communicative features of subjects with Smith-Magenis Syndrome genetic diagnosis.
Procedures: the subjects were two males, 09 and 19 year old. We performed a clinical and laboratory genetic evaluation (FISH assay using probes for the region 17p11.2). The psychological evaluation consisted of behavioral observation and application of the Wechsler Intelligence Scale. Speech evaluation was performed by means of formal and informal procedures and peripheral hearing evaluation.
Results: the clinical genetic analysis showed the phenotypic characteristics of Smith-Magenis syndrome, confirmed by laboratory evaluation. The psychological evaluation revealed the peculiar phenotype behavioral of Smith-Magenis syndrome and confirmed the moderate intellectual disabilities in two subjects. Speech evaluation showed changes in language performance, with changes in phonological, semantic, syntactic and pragmatic levels and psycholinguistic skills, interfering with communication and learning skills. The hearing test showed peripheral hearing within normal parameters.
Conclusion: the multidisciplinary approach made easier the description of clinical, behavioral, cognitive aspects, belonging to the behavioral phenotype of Smith-Magenis syndrome and showed that these changes have severe oral language alterations in skills and psycholinguistic processing of visual and auditory information with remarkable consequences on the development of communicative skills and learning processes.
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Resumo
Tema: o objetivo deste estudo foi descrever os aspectos clínico, comportamental, cognitivo e comunicativo de indivíduos com o diagnóstico genético da Síndrome Smith-Magenis.
Procedimentos: participaram dois indivíduos do sexo masculino, de nove e 19 anos. Realizou-se a avaliação genética clínica e laboratorial (teste FISH, utilizando sonda para região 17p11.2). A avaliação psicológica constou da observação comportamental e aplicação da Escala Wechsler de Inteligência. A avaliação Fonoaudiológica foi realizada por meio de procedimentos formais e informais e avaliação auditiva periférica.
Resultados: a análise genética clínica evidenciou as características fenotípicas da síndrome Smith-Magenis, confirmada pela avaliação laboratorial. A avaliação psicológica evidenciou o fenótipo comportamental peculiar da síndrome Smith-Magenis e comprovou a deficiência intelectual de grau moderado nos dois indivíduos. A avaliação fonoaudiológica mostrou alterações no desempenho linguístico, com alterações nos níveis fonológico, semântico, sintático e pragmático e nas habilidades psicolinguísticas, interferindo nas habilidades comunicativas e de aprendizagem. A avaliação auditiva indicou audição periférica dentro de parâmetros de normalidade.
Conclusão: a avaliação multidisciplinar favoreceu a descrição dos aspectos clínicos, comportamentais, cognitivos que pertencem ao fenótipo comportamental da síndrome Smith-Magenis e permitiu verificar que estes apresentam graves alterações da linguagem oral, das habilidades psicolinguísticas e do processamento das informações visuais e auditivas com reflexos marcantes no desenvolvimento das habilidades comunicativas e processos de aprendizagem.
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References
1. Smith ACM, McGavran L, Waldstein G. Deletion of the 17 short arm in two patients with facial clefts. Am J Hum Genet. 1982; 34:410A.
2. Vlangos CN, Wilson M, Blancato J, Smith ACM, Elsea SH. Diagnostic FISH probes for del 17(p11.2p.11.2) associated with Smith-Magenis syndrome should contin the RAI1 gene. Am J Med Genet A. 2005;132A(3):278-82.
3. Taylor L, Oliver C. The behavioral phenotype of Smith-Magenis syndrome: evidence for a gene-environment interaction. J Intellect Disabil Res. 2008;52(10):830-41.
4. Edelman EA, Girirajan S, Finucane, B, Patel PI, Lupsky JR, Smith ACM, et al. Gender, genotype, and phenotype differences in Smith-Magesis syndrome: a meta-analysis of 105 cases. Clin Genet. 2007;71(6): 540-50.
5. Bronberg R, Ziembar M, Drut M, Goldschmidt E. Smith-Magenis syndrome: comunicacíon de un caso y revision de la bibliografía. Arch Argent Pediatr. 2008;16(2)143-54.
6. Elsea SH, Girirajan S. Smith-Magenis syndrome. Eur J Hum Genet. 2008;16(4):412-21.
7. Taylor L, Oliver C. The behavioral phenotype of Smith-Magenis syndrome: evidence for a gene-environment interaction. J Intellect Disabil Res. 2008;52(10)830-41.
8. Boudreau EA, Johnson KP, Jackman AR, Blancato J, Huizing M, Bendavid C, et al. Review of disrupted sleep patterns in Smith-Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletion. Am J Med Genet A. 2009;149A(7):1382–91.
9. Williams SR, Girirajan S, Tegay D, Nowak N, Hatchwell E, Elsea SH. Array comparative genomic hybridisation of 52 subjects with a Smith-Magenis-like phenotype: identification of dosage sensitive loci also associated with schizophrenia, autism, and developmental delay. J Med Genet. 2010;47(4):223-9.
10. Gropman AL, Duncan WC, Smith AC. Neurologic and developmental features of the Smith-Magenis syndrome (del 17p11.2). Pediatr Neurol. 2006;34(5):337-50.
11. Di Cicco M, Padoan R, Felisati G, Dilani D, Moretti E, Guerneri S, et al. Otorhinolaringologic manifestations of Smith-Magenis syndrome. Int J Pediatr Otorhinolaryngol. 2001;59(2):147-50.
12. Gropman AL, Duncan WC, Smith ACM. Neurological and developmental features of the Smith-Magenis syndrome (del 17p11.2).Pediatric Neurol. 2006;34(5):337-50.
13. Wolters PL, Gropman AL, Martin SC, Smith MR, Hildenbrand HL, Brewer CC, et al. Neurodevelopment of children under 3 years of age with Smith-Magenis syndrome.Pediatr Neurol. 2009;41(4):250-8.
14. Gropman AL, Elsea S, Duncan Junior WC, Smith AC. New developments in Smith-Magenis syndrome (del 17p11.2). Curr Opin Neurol. 2007;20(2):125-34.
15. Martin SC, Wolters PL, Smith ACM. Adaptative and maladaptative behavior in children with Smith-Magenis syndrome. J Autism Dev Disord. 2006;36(4):541-52.
16. Foster RH, Kozachek S, Stern M, Elsea SH. Caring for the caregivers: an investigation of factors related to well-being among parents caring for a child with Smith-Magenis syndrome. J Genet Couns. 2010;19(2):187-98.
17. Madduri N, Peters SU, Voigt RG, Llorent AM, Lupski JR, Potocki, L. Cognitive and adaptive behavior profiles in Smith-Magenis syndrome. J Dev Behav Pediatr. 2006;27(3):188-92.
18. Greenberg G, Lewis RA, Potocki L, Glaze D, Parke J, Killian J, et al. Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2). Am J Med Genet. 1996;62(3):247-54.
19. Liburd N, Ghosh M, Riazuddin S, Naz S, Khan S, Ahmed Z, et al. Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome. Hum Genet. 2001;109(5):535-41.
20. Wechsler D. WISC – escala de inteligência Wechsler para crianças: manual de aplicação. Rio de Janeiro: CEPA; s.d.
21. Wechsler D. Wechsler abbreviated scale of intelligence manual. San Antonio: Psychological Corporation; 1999.
22. Bogossian MADS, Santos MJ. Manual do examinador: teste Illinois de habilidades psicolingüísticas. Rio de Janeiro: EMPSI; 1977.
23. Dunn LM, Padilla ER, Lugo DE, Dunn LM. Test de vocabulario en imagens Peabody: adaptación hispanoamericana. Circle Pines: Dunn Educational Services; 1986.
24. Wertzner HF. Fonologia. In: Andrade CR, Befi-Lopes DM, Fernandes FDM, Wertzner HF. ABFW: teste de linguagem infantil nas áreas de fonologia, vocabulário, fluência e pragmática. 2a. ed. Barueri: Pró-Fono; 2004. p.5-32.
25. Daves H, Silverman SR. Hearing and deafness. New York: Holt; 1970.
Submitted date:
12/14/2010
Accepted date:
05/27/2011
