Disease #06497 (LEUDEN (Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome), OMIM:618877)

Official abbreviation LEUDEN
Name Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome
OMIM ID 618877
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene EIF2AK2
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00421985 208327 - - F no Germany - - - - - LEUDEN Delayed CNS myelination, Microcephaly, Absent speech, Motor delay, Ataxia, Dystonia, Spasticity, Hypoplasia of the corpus callosum, Growth delay, Short stature EIF2AK2 EIF2AK2 1 1 Andreas Laner
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