Concept information
Término preferido
DiGeorge syndrome
Definición
- DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by the deletion of a small segment of chromosome 22. While the symptoms can vary, they often include congenital heart problems, specific facial features, frequent infections, developmental delay, learning problems and cleft palate. (Wikipedia)
Concepto genérico
Etiquetas alternativas
- velocardiofacial syndrome
En otras lenguas
-
francés
-
syndrome vélocardiofacial
URI
http://data.loterre.fr/ark:/67375/VH8-N0JB9FMQ-0
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