Parkinsonism-dystonia, infantile

rare

Infantile dystonia-parkinsonism (IPD) is an extremely rare inherited neurological syndrome that presents in early infancy with hypokinetic parkinsonism and dystonia and that can be fatal.

Identifiers: MONDO:0013150 Orphanet:238455
Part of: Combined dystonia Parkinsonian disorder Syndromic disease
Also known as: IPD · PKDYS

Subtypes

All diseases Rare only

Disease	ID	Genes
Brain dopamine-serotonin vesicular transport disease	MONDO:0018130	SLC18A2
Classic dopamine transporter deficiency syndrome	MONDO:0054835
Parkinsonism-dystonia 3, childhood-onset	MONDO:0030676	WARS2

Rare disease

Projects

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