Síndrome de Coffin-Siris: relato de caso / Coffin-Siris syndrome: case report
Pediatria (Säo Paulo)
;
32(2): 148-150, abr.-jun. 2010. ilus
Article
in Portuguese
| LILACS
| ID: lil-570047
RESUMO
Objetivo: Apresentar o caso clínico de ummenino de 4 anos com Síndrome de Coffin-Siris.Relato do caso: O paciente apresentava retardo decrescimento pós-natal, face grosseira, sobrancelhascheias, nariz alargado, filtro longo, boca larga, criptorquidiae hipoplasia da unha do quinto dedo. Ocariótipo em sangue periférico foi normal, 46 XY.Conclusão: As características clínicas do pacientesão consistentes com o diagnóstico da Síndromede Coffin-Siris, uma doença genética em que hámenos de 100 casos descritos.
ABSTRACT
Objective: To report the clinical case of 4 yearsold boy with Coffin-Siris syndrome. Case report:The patient presented post natal growth retardation,coarse facies, brushy eyebrows, broad nose, long philtrum,wide mouth, cryptorchidism and hypoplastic 5thfingernails. The blood cariotype was normal, 46XY.Conclusions: The clinical characteristics are consistentwith the diagnosis of Coffin-Siris syndrome, agenetic disorder of which there are less than 100 casesreported.
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Index:
LILACS (Americas)
Main subject:
Quality of Life
/
Diagnostic Imaging
/
Chromosomes
/
Genetic Predisposition to Disease
/
Genetic Counseling
Type of study:
Diagnostic study
Limits:
Adolescent
/
Humans
/
Male
Language:
Portuguese
Journal:
Pediatria (Säo Paulo)
Journal subject:
Pediatrics
Year:
2010
Type:
Article
Affiliation country:
Brazil
Institution/Affiliation country:
Hospital Infantil Albert Sabin/BR
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