Aprosencephaly/atelencephaly spectrum

Orpha code: 566847OMIM code:

Definicja

A group of rare central nervous system malformations characterized by varying degrees of absence or dysplasia of the derivatives of the prosencephalon (i. e. telencephalon and diencephalon), with an intact cranial vault. The spectrum comprises atelencephaly, the less severe form, in which only the telencephalon is affected, and aprosencephaly, where the diencephalon is also involved. The malformations may occur in an isolated form or in association with other anomalies.

Disease data
Klasyfikacja

Morphological anomaly

Synonimy
AP/AT spectum
AP/AT spectum
Kod ORPHA
566847
Kod OMIM
-
Kod ICD10
-
Kod ICD11
-

No additional description.

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