Rhombencephalosynapsis presenting antenatally with ventriculomegaly/hydrocephalus in a likely case of Gomez-López-Hernández syndrome.
Clin Dysmorphol
; 16(1): 21-25, 2007 Jan.
Article
en En
| MEDLINE
| ID: mdl-17159510
Rhombencephalosynapsis is a rare cerebellar malformation that can be associated with anomalies of the cerebral hemispheres and variable degrees of neurodevelopmental delay. A syndromic association, comprising rhombencephalosynapsis, developmental delay, scalp alopecia and trigeminal anaesthesia (Gomez-López-Hernández syndrome) has been described in seven individuals. We report the case of a 2-year-old boy with rhombencephalosynapsis, and review the evidence for a possible diagnosis of Gomez-López-Hernández syndrome. We also discuss other malformations reported in combination with rhombencephalosynapsis, and consider the possibility that a genetic aetiology for syndromic and nonsyndromic forms of rhombencephalosynapsis may be established with more detailed clinical and genetic studies.
Texto completo:
1
Bases de datos:
MEDLINE
Asunto principal:
Rombencéfalo
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Discapacidades del Desarrollo
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Anomalías Craneofaciales
/
Hidrocefalia
Tipo de estudio:
Diagnostic_studies
Límite:
Humans
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Infant
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Male
Idioma:
En
Revista:
Clin Dysmorphol
Asunto de la revista:
TERATOLOGIA
Año:
2007
Tipo del documento:
Article
País de afiliación:
Irlanda