Artigo Revisado por pares

Cerebrocostomandibular Syndrome

1985; SAGE Publishing; Volume: 24; Issue: 4 Linguagem: Inglês

10.1177/000992288502400411

ISSN

1938-2707

Autores

Kim Smith, K. Sekar,

Tópico(s)

Fetal and Pediatric Neurological Disorders

Resumo

Cerebrocostomandibular syndrome (CCM) is characterized by micrognathia, cleft palate, rib defects, and frequently, mental deficiency. Death from respiratory complications occurs in 40 percent of cases before they reach 1 year of age. We describe a case of CCM with the previously unreported findings of large for gestational age at birth, radiologic evidence of bilaterally displaced radial heads, and development of brachycephaly.

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