Atypical Pantothenate Kinase-associated Neurodegeneration
Genes related to Atypical Pantothenate Kinase-associated Neurodegeneration
- PANK2
 
Clinical Features
Top most frequent phenotypes and symptoms related to Atypical Pantothenate Kinase-associated Neurodegeneration
- Spasticity
 - Cognitive impairment
 - Hyperreflexia
 - Dysarthria
 - Optic atrophy
 - Tremor
 - Gait disturbance
 - Dysphagia
 - Blindness
 - Depressivity
 
And another 20 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Atypical Pantothenate Kinase-associated Neurodegeneration Is also known as neurodegeneration with brain iron accumulation type 1, atypical form, pkan, atypical form, nbia1, atypical form.
Researches and researchers
Doctors, researchs, and experts related to Atypical Pantothenate Kinase-associated Neurodegeneration extracted from public data.
Atypical Pantothenate Kinase-associated Neurodegeneration Experts map
Current Researchs and researchers
- 
Investigator of research project
 MILANO — Pr Sonia LEVI 
- 
Institution/s:
— Università Vita e Salute, IRCCS Ospedale San Raffaele - 
Research area/topic::
Implementation of human neuronal cultures and mouse models of Pantothenate kinase 2 deficiency to investigate pathogenic mechanisms of iron-related neurodegeneration and evaluate Coenzyme A therapeutic efficacy
 
 - 
Institution/s:
 
Atypical Pantothenate Kinase-associated Neurodegeneration Recommended genes panels
| Panel Name, Specifity and genes Tested/covered | 
|---|
 	MitoMet®Plus aCGH Analysis.
By Baylor Miraca Genetics Laboratories (United States). 
RGS9, RHO, GRK1, RLBP1, RNASEL, BCS1L, RP1, RP2, RP9, RPE65, RPGR, RPL35A, MRPL3, RPS14, RS1, SAG, SARDH, SCO2, SCP2, SDHB	, (...)
 
View the complete list with 612 more genes 
Specificity
 
1 % 
Genes
 
100 %  | 
 	Epilepsy Advanced Sequencing and CNV Evaluation.
By Athena Diagnostics Inc (United States). 
SCN1A, SCN1B, SCN2A, SCN3A, SCN5A, SCN8A, SCN9A, SHH, ST3GAL3, ST3GAL5, STIL, SIX3, SLC2A1, SLC35A2, SLC6A1, SLC6A8, SLC9A6, SMC1A, KDM5C, SMS	, (...)
 
View the complete list with 214 more genes 
Specificity
 
1 % 
Genes
 
100 %  | 
 	Epilepsy Advanced Sequencing and CNV Evaluation - Syndromic Disorders.
By Athena Diagnostics Inc (United States). 
SYNGAP1, TBX1, TSC1, TSC2, SETBP1, PANK2, ADGRV1, ATP6V0A2, MAGI2, VPS13A, ANKRD11, VPS13B, KIF1BP, KANSL1, SMC3, PIGV, NIPBL, ROGDI, GFAP, HPRT1	, (...)
 
View the complete list with 11 more genes 
Specificity
 
4 % 
Genes
 
100 %  | 
 	Pantothenate Kinase Associated Neurodegeneration (PKAN), PANK2, Deletion/Duplication.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). 
PANK2
 
Specificity
 
100 % 
Genes
 
100 %  | 
 	Pantothenate Kinase Associated Neurodegeneration (PKAN), PANK2, Sequencing and Deletion/Duplication.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). 
PANK2
 
Specificity
 
100 % 
Genes
 
100 %  | 
 	Neurodegeneration with Brain Iron Accumulation (NBIA) Panel, Sequencing.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). 
SQSTM1, PANK2, TRIM32, FA2H, CP, C19orf12, DCAF17, WDR45, COASY, ATP13A2, FTL, FUCA1, KIF1A, PLA2G6
 
Specificity
 
8 % 
Genes
 
100 %  | 
 	Dystonia.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). 
SCP2, SGCE, SLC20A2, SLC2A1, SLC6A3, SPR, SUCLA2, SUOX, TAF1, TH, TIMM8A, TREX1, MCOLN1, FBXO7, CACNA1A, NPC2, PINK1, PANK2, SAMHD1, APTX	, (...)
 
View the complete list with 57 more genes 
Specificity
 
2 % 
Genes
 
100 %  | 
 	Movement Disorders Panel.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). 
SCP2, SGCE, SLC20A2, SLC2A1, SLC6A3, SNCA, SPR, SQSTM1, SUCLA2, SUOX, TAF1, TH, TIMM8A, TREX1, MCOLN1, VPS35, FBXO7, CACNA1A, NPC2, PINK1	, (...)
 
View the complete list with 72 more genes 
Specificity
 
2 % 
Genes
 
100 %  | 
You can get up to 94 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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	MitoMet®Plus aCGH Analysis.