"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatment.
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.
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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