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Atypical pantothenate kinase-associated neurodegeneration
ORPHA:216873
Classification level: Subtype of disorder- Synonym(s):
- NBIA1, atypical form
- Neurodegeneration with brain iron accumulation type 1, atypical form
- PKAN, atypical form
- Prevalence: -
- Inheritance: -
- Age of onset: -
- ICD-10: G23.0
- OMIM: 234200
- UMLS: -
- MeSH: -
- GARD: -
- MedDRA: -
Summary
This disease is described under Pantothenate kinase-associated neurodegeneration
A summary on this disease is available in
Detailed information
General public
- Article for general public
- Svenska (2012) - Socialstyrelsen
- Deutsch (2017, pdf) - ACHSE
Guidelines
- Clinical practice guidelines
- English (2017) - Mol Genet Metab
- Anesthesia guidelines
- Czech (2016) - Orphananesthesia
- English (2016) - Orphananesthesia
Disease review articles
- Review article
- English (2011) - Orphanet J Rare Dis
- Clinical genetics review
- English (2017) - GeneReviews


Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.