Disease #00896 (DWS (Dandy-Walker syndrome (DWS)), OMIM:220200)

Official abbreviation DWS
Name Dandy-Walker syndrome (DWS)
OMIM ID 220200
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 2 genes ZIC1, ZIC4
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00473530 Fam9116875Pat907 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history F yes Iran - - - - - DWS Developmental delay, severe; Speech delay; Mental retardation, moderate to severe; Seizures; Microcephaly; Hypotonia; Agitation; Micrognathia; Strabismus; Optic atrophy, bilateral; Early eruption of teeth; Large ears; Joints laxity; Flexed elbow; Extended feet; Feeding problem and very thin built. Brain MRI revealed hypoplasia of inferior vermis suggestive of dandy walker spectrum - COQ4 1 1 Johan den Dunnen
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