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"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatment.
Lalatta, F; Clerici Bagozzi, D; Salmoiraghi, M G; Tagliabue, P; Tischer, C; Zollino, M; Di Rocco, C; Neri, G; Opitz, J M.
Afiliación
  • Lalatta F; Seconda Clinica Pediatrica, Università di Milano, Italy.
Am J Med Genet ; 37(4): 451-6, 1990 Dec.
Article en En | MEDLINE | ID: mdl-2260586
ABSTRACT
We report on 3 new cases of C trigonocephaly syndrome. In addition to the findings characteristic of this condition, one of the patients also had a large omphalocele. This patient was referred from a suburban hospital with a diagnosis of Down syndrome, stressing the fact that C syndrome is still under-recognized and underdiagnosed. Another patient was diagnosed at birth and immediately submitted to craniosynostectomy. A second operation was performed 7 months later resulting in normal brain growth and close to normal psychomotor development at 3 years, in contrast to the third patient, who was not treated surgically and was severely retarded at 4 years.
Asunto(s)
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cráneo / Anomalías Múltiples / Craneosinostosis / Discapacidad Intelectual Límite: Child, preschool / Female / Humans / Male / Newborn País/Región como asunto: Europa Idioma: En Revista: Am J Med Genet Año: 1990 Tipo del documento: Article País de afiliación: Italia
Buscar en Google
Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cráneo / Anomalías Múltiples / Craneosinostosis / Discapacidad Intelectual Límite: Child, preschool / Female / Humans / Male / Newborn País/Región como asunto: Europa Idioma: En Revista: Am J Med Genet Año: 1990 Tipo del documento: Article País de afiliación: Italia