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Hydrolethalus syndrome: report of an apparent mild case, literature review, and differential diagnosis.
Aughton, D J; Cassidy, S B.
Afiliación
  • Aughton DJ; Department of Pediatrics, University of Connecticut School of Medicine, Farmington 06032-9984.
Am J Med Genet ; 27(4): 935-42, 1987 Aug.
Article en En | MEDLINE | ID: mdl-3321994
ABSTRACT
We present an infant with manifestations of the hydrolethalus syndrome who has survived for over 5 months; previously, the longest survival reported in this condition has been 2 days. The literature is reviewed and the clinical and pathological findings of our patient are compared with those of the 50 previously reported cases. The differential diagnosis of the condition is discussed.
Asunto(s)
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Fisura del Paladar / Encefalocele / Agenesia del Cuerpo Calloso / Hidrocefalia / Micrognatismo Tipo de estudio: Diagnostic_studies / Systematic_reviews Límite: Humans / Infant / Male Idioma: En Revista: Am J Med Genet Año: 1987 Tipo del documento: Article
Buscar en Google
Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Fisura del Paladar / Encefalocele / Agenesia del Cuerpo Calloso / Hidrocefalia / Micrognatismo Tipo de estudio: Diagnostic_studies / Systematic_reviews Límite: Humans / Infant / Male Idioma: En Revista: Am J Med Genet Año: 1987 Tipo del documento: Article