X-linked lissencephaly - agenesis of corpus callosum - genital anomalies (Q57547): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/714984818 / rank | |||
Normal rank | |||
Revision as of 05:11, 14 August 2026
X-linked lissencephaly with abnormal genitalia (XLAG) is a severe neurological disorder that only manifests in males and includes lissencephaly with posterior-to-anterior gradient and only moderate increase in thickness of the cortex, absent corpus callosum, neonatal-onset severe epilepsy, hypothalamic dysfunction including defective temperature regulation, and ambiguous genitalia with micropenis and cryptorchidism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_714984818 |
||
| English | X-linked lissencephaly - agenesis of corpus callosum - genital anomalies |
X-linked lissencephaly with abnormal genitalia (XLAG) is a severe neurological disorder that only manifests in males and includes lissencephaly with posterior-to-anterior gradient and only moderate increase in thickness of the cortex, absent corpus callosum, neonatal-onset severe epilepsy, hypothalamic dysfunction including defective temperature regulation, and ambiguous genitalia with micropenis and cryptorchidism. |
