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Newly recognized syndrome of cerebral, ocular, dental, auricular, skeletal anomalies: CODAS syndrome--a case report.
Shebib, S M; Reed, M H; Shuckett, E P; Cross, H G; Perry, J B; Chudley, A E.
Afiliação
  • Shebib SM; Department of Pediatrics and Child Health, University of Manitoba, Canada.
Am J Med Genet ; 40(1): 88-93, 1991 Jul 01.
Article em En | MEDLINE | ID: mdl-1887855
We report on a child with a unique constellation of congenital anomalies suggesting a new syndrome. These consist of developmental delay; craniofacial abnormalities, including bilateral cataracts, ptosis, median nasal groove, malformed ears with associated neurosensory hearing loss; dental anomalies consisting of anomalous cusp morphology with unusual pointed extensions and delayed tooth eruption; short stature with marked delay in epiphyseal ossification; coronal clefts involving vertebrae T11-S2; and dislocated hips. A literature search and use of a computer-assisted syndrome-identification program failed to uncover an identical case.
Assuntos
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Bases de dados: MEDLINE Assunto principal: Anormalidades Múltiplas Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Infant Idioma: En Revista: Am J Med Genet Ano de publicação: 1991 Tipo de documento: Article País de afiliação: Canadá
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Bases de dados: MEDLINE Assunto principal: Anormalidades Múltiplas Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Infant Idioma: En Revista: Am J Med Genet Ano de publicação: 1991 Tipo de documento: Article País de afiliação: Canadá