Basal Ganglia Calcification, Idiopathic, 1; Ibgc1

Description

Familial idiopathic basal ganglia calcification is an autosomal dominant condition characterized by symmetric calcification in the basal ganglia and other brain regions. Patients with calcifications can either be asymptomatic or show a wide spectrum of neuropsychiatric symptoms, including parkinsonism, dystonia, tremor, ataxia, dementia, psychosis, seizures, and chronic headache. Serum levels of calcium, phosphate, alkaline phosphatase, and parathyroid hormone are normal. The typical age at clinical onset is between 30 and 50 years (summary by Wang et al., 2012).Calcification of the basal ganglia is a nonspecific finding in many medical conditions, including infectious, metabolic, and genetic syndromes. In addition, calcification of the basal ganglia is observed as an incidental finding in approximately 0.7 to 1.2% of CT scans (Koller et al., 1979; Harrington et al., 1981; Forstl et al., 1992). These incidental calcifications are usually benign and have no clear etiology, especially in patients over 60 years of age (Geschwind et al., 1999). Forstl et al. (1992) found no increased risk for dementia, cerebral infarction, seizures, alcoholism, vertigo, or headache in 166 patients with calcification of the basal ganglia compared to 622 individuals without calcification. Genetic Heterogeneity of Idiopathic Basal Ganglia CalcificationIBGC2 (OMIM ) has been mapped to chromosome 2q37. IBGC4 (OMIM ) is caused by mutation in the PDGFRB gene (OMIM ) on chromosome 5q32; IBGC5 (OMIM ) is caused by mutation in the PDGFB gene (OMIM ) on chromosome 22q13; and IBGC6 (OMIM ) is caused by mutation in the XPR1 gene (OMIM ) on 1q25.See {114100} for a childhood-onset form of idiopathic basal ganglia calcification.The symbol IBGC3 previously referred to the locus on chromosome 8p11 that includes the SLC20A2 gene (Dai et al., 2010). However, the family that originally defined the putative IBGC1 locus on chromosome 14q (Geschwind et al., 1999) was later found to carry a pathogenic mutation in the SLC20A2 gene (Hsu et al., 2013), and the IBGC locus on chromosome 14q has not been replicated (Oliveira et al., 2004; Hsu et al., 2013). Thus, the symbol IBGC1 now refers to the disorder caused by mutation in the SLC20A2 gene on chromosome 8p11 and the symbol IBGC3 is no longer used.

Clinical Features

Top most frequent phenotypes and symptoms related to Basal Ganglia Calcification, Idiopathic, 1; Ibgc1

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Microcephaly
  • Ataxia
  • Motor delay
  • Milia
  • Cognitive impairment
  • Hepatomegaly
  • Pain
And another 63 symptoms. If you need more information about this disease we can help you.
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Incidence and onset information

Not enough data available about incidence and published cases.


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Basal Ganglia Calcification, Idiopathic, 1; Ibgc1 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Dystonia Exome Panel.

By Genetic Services Laboratory University of Chicago in United States.

AARS2, UQCRQ, ATP7B, AUH, BCS1L, PSEN1, GLB1, HPRT1, POLG, NDUFS4, AFG3L2, FOXRED1, NDUFAF2, PANK2, MECP2, NDUFA12, NDUFA9, TTC19, NDUFA10, SCP2 , (...)

View the complete list with 150 more genes
Specificity
3 %
Genes
100 %
PDGFB. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

PDGFB
Specificity
100 %
Genes
25 %
Dermatofibrosarcoma protuberans (sequence analysis of PDGFB gene).

By CGC Genetics in Portugal.

PDGFB
Specificity
100 %
Genes
25 %
Idiopathic Basal Ganglia Calcification Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

SLC20A2, PDGFRB, PDGFB, XPR1
Specificity
100 %
Genes
100 %
Neurogenetic Disorders - panels.

By MGZ Medical Genetics Center in Germany.

MTHFR, TTR, UBE3A, AARS2, ABHD12, ACAD9, ACADM, ACADS, AGL, ACADVL, YARS2, PC, UQCRQ, ARG1, UQCRB, ATP5F1E, ATP7B, ATPAF2, AUH, BCKDHA , (...)

View the complete list with 577 more genes
Specificity
1 %
Genes
25 %
Dermatofibrosarcoma protuberans.

By Centogene AG - the Rare Disease Company in Germany.

PDGFB
Specificity
100 %
Genes
25 %
Basal ganglia calcification Panel.

By CeGaT GmbH in Germany.

TYROBP, POLG, PANK2, CA2, GALC, AIRE, BRAF, FOLR1, COL4A1, SAMHD1, RNASEH2A, RNASEH2C, RNASEH2B, TREX1, GFAP, GATA3, ERCC6, IFIH1, ADAR, CTC1 , (...)

View the complete list with 7 more genes
Specificity
15 %
Genes
100 %
FAMILIAL MULTIPLE MENINGIOMA.

By Hereditary Cancer Group - Genetic Diagnostic Unit Germans Trias I Pujol Research Institute in Spain.

PTEN, NF2, SUFU, SMARCE1, PDGFB, MN1
Specificity
17 %
Genes
25 %
Fahr’s disease.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

SLC20A2, PDGFRB, PDGFB
Specificity
100 %
Genes
75 %
PDGFB.

By Fulgent Genetics Fulgent Genetics in United States.

PDGFB
Specificity
100 %
Genes
25 %
Parkinson Disease Panel.

By Blueprint Genetics in Finland.

SPR, PARK7, PINK1, PRKN, TH, PLA2G6, MAPT, GCH1, LRRK2, SNCA, ATP1A3, SYNJ1, ATP13A2, VPS13A, SLC20A2, FBXO7, SLC6A3, VPS35, PRKRA, PDGFRB , (...)

View the complete list with 2 more genes
Specificity
14 %
Genes
75 %
Dystonia Panel.

By Blueprint Genetics in Finland.

SPR, PNKD, SLC2A1, TH, TOR1A, THAP1, GCH1, SGCE, FA2H, ATP1A3, PRRT2, DCAF17, PRKRA, PDGFRB, PDGFB, KMT2B, ANO3, BCAP31, GNAL, ADCY5
Specificity
10 %
Genes
50 %
Caris MI TumorSeek 592-Gene NGS Panel.

By Caris Life Sciences in United States.

BRCA1, BRCA2, VHL, APC, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, FOXL2, HNF1A, PPARG, COL1A1, WT1, RB1, SDHAF2 , (...)

View the complete list with 571 more genes
Specificity
1 %
Genes
50 %
BILATERAL STRIOPALLIDODENTATE CALCINOSIS (BSPDC).

By Laboratorio de Genetica Clinica SL in Spain.

SLC20A2, PDGFRB, PDGFB
Specificity
100 %
Genes
75 %
Fahr Disease , Panel massive Sequencing (NGS) (SLC20A2, PDGFRB, PDGFB) Genes.

By Reference Laboratory Genetics in Spain.

SLC20A2, PDGFRB, PDGFB
Specificity
100 %
Genes
75 %
Schwannomatosis, Panel Massive Sequencing (NGS) 7 Genes.

By Reference Laboratory Genetics in Spain.

PTEN, NF2, SUFU, LZTR1, SMARCE1, SMARCB1, PDGFB
Specificity
15 %
Genes
25 %
Familial Meningioma , Panel Massive Sequencing (NGS) 6 Genes.

By Reference Laboratory Genetics in Spain.

PTEN, NF2, SUFU, SMARCE1, PDGFB, MN1
Specificity
17 %
Genes
25 %
Tempus xO assay.

By Tempus Labs, Inc. in United States.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, ABCB11, ABCB4, FKBP10, FOXL2, HNF1A, PPARG , (...)

View the complete list with 1693 more genes
Specificity
1 %
Genes
50 %
Primary Familial Brain Calcification: gene sequencing panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

SLC20A2, PDGFRB, PDGFB, XPR1
Specificity
100 %
Genes
100 %
Primary Familial Brain Calcification: gene deletion/duplication panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

SLC20A2, PDGFB
Specificity
100 %
Genes
50 %
PDGFRB. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

PDGFRB
Specificity
100 %
Genes
25 %
Myeloproliferative disorder with eosinophilia (sequence analysis of PDGFRB gene).

By CGC Genetics in Portugal.

PDGFRB
Specificity
100 %
Genes
25 %
RT-PCR t(5;12) (TEL/PDGFRb).

By CGC Genetics in Portugal.

ETV6, PDGFRB
Specificity
50 %
Genes
25 %
Basal ganglia calcification, idiopathic 1 (sequence anaysis of PDGFRB gene).

By CGC Genetics in Portugal.

PDGFRB
Specificity
100 %
Genes
25 %
Detection by FISH of PDGFRB (5q32) rearrangements.

By CGC Genetics in Portugal.

PDGFRB
Specificity
100 %
Genes
25 %
Infantile myofibromatosis 1 (sequence analysis of PDGFRB gene).

By CGC Genetics in Portugal.

PDGFRB
Specificity
100 %
Genes
25 %
Infantile Neurofibromatosis and Idiopathic Basal Ganglia Calcification via the PDGFRB Gene.

By PreventionGenetics PreventionGenetics in United States.

PDGFRB
Specificity
100 %
Genes
25 %
Infantile Myofibromatosis Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

NOTCH3, PDGFRB
Specificity
50 %
Genes
25 %
Overgrowth syndrome NGS panel.

By Connective Tissue Gene Tests in United States.

FBN1, NSD1, GPC3, SETD2, PIGA, OFD1, DNMT3A, NFIX, EZH2, PDGFRB, EED
Specificity
10 %
Genes
25 %
Overgrowth syndrome Comprehensive panel.

By Connective Tissue Gene Tests in United States.

FBN1, NSD1, GPC3, SETD2, PIGA, OFD1, DNMT3A, NFIX, EZH2, PDGFRB, EED
Specificity
10 %
Genes
25 %
Overgrowth syndrome Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

FBN1, NSD1, GPC3, SETD2, PIGA, OFD1, DNMT3A, NFIX, EZH2, PDGFRB, EED
Specificity
10 %
Genes
25 %
Progeroid syndromes and related disorders NGS panel.

By Connective Tissue Gene Tests in United States.

RECQL4, B4GALT7, PYCR1, FBN1, ALDH18A1, LMNA, BSCL2, ERCC2, ERCC3, ZMPSTE24, ERCC6, ERCC4, B3GALT6, POLD1, ERCC8, AGPAT2, WRN, PDGFRB, ERCC5, BANF1 , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
25 %
Progeroid syndromes and related disorders Comprehensive panel.

By Connective Tissue Gene Tests in United States.

RECQL4, B4GALT7, PYCR1, FBN1, ALDH18A1, LMNA, BSCL2, ERCC2, ERCC3, ZMPSTE24, ERCC6, ERCC4, B3GALT6, POLD1, ERCC8, AGPAT2, WRN, PDGFRB, ERCC5, BANF1 , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
25 %
Progeroid syndromes and related disorders Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

RECQL4, B4GALT7, PYCR1, FBN1, ALDH18A1, LMNA, BSCL2, ERCC2, ERCC3, ZMPSTE24, ERCC6, ERCC4, B3GALT6, POLD1, ERCC8, AGPAT2, WRN, PDGFRB, ERCC5, BANF1 , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
25 %
Custom solid tumor gene sequencing panel.

By Molecular Diagnostics Laboratory University Health Network in Canada.

APC, PTEN, TP53, FOXL2, TYRP1, RET, RAF1, BRAF, HRAS, KRAS, MAP2K1, NRAS, CDK4, CDKN2A, MET, NF1, GRIN2A, HGF, ERCC2, CTNNB1 , (...)

View the complete list with 25 more genes
Specificity
3 %
Genes
25 %
Cancer Hotspot Panel.

By Centogene AG - the Rare Disease Company in Germany.

BRCA1, BRCA2, VHL, APC, MLH1, PTEN, TP53, HNF1A, RB1, RET, GNAT2, IDH2, FGFR3, AR, BRAF, HRAS, KRAS, NRAS, PTPN11, FGFR2 , (...)

View the complete list with 68 more genes
Specificity
2 %
Genes
25 %
Solid Tumor Panel.

By Centogene AG - the Rare Disease Company in Germany.

VHL, APC, MLH1, PTEN, TP53, RB1, RET, IDH2, FGFR3, AR, BRAF, HRAS, KRAS, MAP2K1, NRAS, PTPN11, FGFR2, TSC1, ALK, ATM , (...)

View the complete list with 42 more genes
Specificity
2 %
Genes
25 %
Myeloproliferative disorder, chronic, with eosinophilia.

By Centogene AG - the Rare Disease Company in Germany.

PDGFRB
Specificity
100 %
Genes
25 %
Fluorescent in situ Hybridization - Hematopathology.

By Hartford Hospital Laboratory - Molecular Genetics and Cytogenetics Hartford Hospital-Hartford-CT-USA in United States.

RUNX1, TP53, RB1, ATM, CDKN2A, FGFR1, KMT2A, IGH, JAK2, ABL1, PDGFRA, ETV6, BCR, RUNX1T1, PDGFRB, BCL2, PML, CBFB, RARA, TCF3 , (...)

View the complete list with 9 more genes
Specificity
4 %
Genes
25 %
Disorders associated with malignancy Panel.

By CeGaT GmbH in Germany.

MSH2, PMS2, MSH6, MLH1, PTEN, RECQL4, SDHB, BLM, TINF2, TSC2, TSC1, ATM, PTCH1, NF2, STK11, SDHD, FLCN, PRKAR1A, RTEL1, NF1 , (...)

View the complete list with 25 more genes
Specificity
3 %
Genes
25 %
Platelets, Coagulation disorders Panel.

By CeGaT GmbH in Germany.

F2, F5, VHL, ENTPD1, F11, VWF, F8, ADAMTS13, SERPINE1, TET2, ETV6, PDGFRB, F10, F12, DSG1, F13A1, SERPINC1
Specificity
6 %
Genes
25 %
Dystonia: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

PTEN, ATP7B, AUH, PSEN1, HPRT1, AFG3L2, FOXRED1, PANK2, SCP2, GAMT, SPR, SUCLA2, PINK1, TIMM8A, MMADHC, SUOX, PTS, QDPR, MPV17, SDHAF1 , (...)

View the complete list with 62 more genes
Specificity
3 %
Genes
50 %
PDGFRB.

By Fulgent Genetics Fulgent Genetics in United States.

PDGFRB
Specificity
100 %
Genes
25 %
Onco microarray for ALL.

By Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center in United States.

TP53, RB1, CDKN2A, PAX5, JAK2, IKZF1, ETV6, PDGFRB, EBF1, BTG1
Specificity
10 %
Genes
25 %
Onco microarray for MDS/AML.

By Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center in United States.

RUNX1, TP53, WT1, IDH2, KRAS, NRAS, PTPN11, CBL, ALK, GATA2, NF1, FUS, GATA1, DNMT3A, EZH2, TFG, TERT, KMT2A, KIT, ASXL1 , (...)

View the complete list with 40 more genes
Specificity
2 %
Genes
25 %
Focus::Renal® NGS Panel.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

VHL, PTEN, TP53, RAF1, BRAF, TSC2, TSC1, ALK, PTCH1, MET, FGFR1, SETD2, KDM5C, MTOR, ARID1A, KIT, BAP1, PIK3CA, AKT2, FLT3 , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
25 %
Solid Tumor Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

BRCA1, BRCA2, VHL, APC, MLH1, PTEN, TP53, FOXL2, PPARG, WT1, RB1, RET, RAF1, IDH2, FGFR3, AR, BRAF, CREBBP, HRAS, KRAS , (...)

View the complete list with 102 more genes
Specificity
1 %
Genes
25 %
Hematopoietic Disorders Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

RUNX1, TP53, IDH2, BCOR, BRAF, CREBBP, KRAS, NRAS, PTPN11, CBL, NSD1, ATM, GATA2, PAX5, CEBPA, MPL, NF1, SETBP1, GATA3, GATA1 , (...)

View the complete list with 34 more genes
Specificity
2 %
Genes
25 %
Melanoma Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

PTEN, TP53, RB1, RET, FGFR3, BRAF, HRAS, KRAS, MAP2K1, NRAS, FGFR2, MAP2K2, ALK, CDK4, CDKN2A, MET, NF1, FGFR1, KMT2D, MED12 , (...)

View the complete list with 18 more genes
Specificity
3 %
Genes
25 %
FoundationOne® Heme.

By Foundation Medicine, Inc. in United States.

BRCA1, BRCA2, VHL, APC, MSH2, MSH6, MLH1, MUTYH, PTEN, RUNX1, TP53, PC, FOXL2, HNF1A, WT1, RB1, RET, TNFRSF11A, CPS1, SDHC , (...)

View the complete list with 385 more genes
Specificity
1 %
Genes
25 %
NeoTYPE® Discovery Profile for Solid Tumors.

By NeoGenomics Laboratories NeoGenomics Laboratories, Inc. in United States.

BRCA1, BRCA2, VHL, APC, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RUNX1, TP53, FOXL2, HNF1A, WT1, RB1, RET, SDHC, RAF1, FH , (...)

View the complete list with 295 more genes
Specificity
1 %
Genes
25 %
Infantile Myofibromatosis Type 1 , Sequencing PDGFRB Gene.

By Reference Laboratory Genetics in Spain.

PDGFRB
Specificity
100 %
Genes
25 %
152 Integrated Advantage NGS Solid Tumor Panel.

By Integrated Molecular Diagnostics Pathology, Inc. in United States.

BRCA1, BRCA2, MTHFR, VHL, APC, MLH1, PTEN, TP53, RB1, RET, RAF1, IDH2, TYMP, STAT3, FGFR3, AR, FANCC, BRAF, HRAS, KRAS , (...)

View the complete list with 132 more genes
Specificity
1 %
Genes
25 %
Tempus xT assay.

By Tempus Labs, Inc. in United States.

BRCA1, BRCA2, MTHFR, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, ATP7B, FOXL2, HNF1A, WT1, RB1 , (...)

View the complete list with 571 more genes
Specificity
1 %
Genes
25 %
Basal ganglia calcification type 6, idiopathic.

By Centogene AG - the Rare Disease Company in Germany.

XPR1
Specificity
100 %
Genes
25 %
Single gene testing XPR1.

By CeGaT GmbH in Germany.

XPR1
Specificity
100 %
Genes
25 %
XPR1.

By Fulgent Genetics Fulgent Genetics in United States.

XPR1
Specificity
100 %
Genes
25 %
Primary Familial Brain Calcification Type 6 , Sequencing XPR1 Gene.

By Reference Laboratory Genetics in Spain.

XPR1
Specificity
100 %
Genes
25 %
Dystonia.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

PTEN, ATP7B, AUH, PSEN1, HPRT1, AFG3L2, FOXRED1, PANK2, SCP2, GAMT, SPR, SUCLA2, PINK1, TIMM8A, MMADHC, SUOX, PTS, QDPR, MPV17, SDHAF1 , (...)

View the complete list with 57 more genes
Specificity
2 %
Genes
25 %
Movement Disorders Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

PTEN, ATP7B, AUH, PSEN1, HPRT1, TRIM32, POLG, AFG3L2, FOXRED1, PANK2, SCP2, GAMT, SPR, SUCLA2, PARK7, PINK1, SQSTM1, TIMM8A, MMADHC, SUOX , (...)

View the complete list with 72 more genes
Specificity
2 %
Genes
25 %
Ataxia Exome Panel.

By Genetic Services Laboratory University of Chicago in United States.

FMR1, TTR, UBE3A, AARS2, ABHD12, PC, UQCRQ, UQCRB, HLCS, BTD, ATP7B, ATPAF2, AUH, BCKDHA, BCKDHB, BCS1L, TWNK, C12orf65, ADSL, PRKCG , (...)

View the complete list with 460 more genes
Specificity
1 %
Genes
25 %
SLC20A2. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

SLC20A2
Specificity
100 %
Genes
25 %
Basal ganglia calcification, idiopathic 1 (sequence anaysis of SLC20A2 gene).

By CGC Genetics in Portugal.

SLC20A2
Specificity
100 %
Genes
25 %
Idiopathic basal ganglia calcification 1.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

SLC20A2
Specificity
100 %
Genes
25 %
Basal ganglia calcification, idiopathic, 3.

By Centogene AG - the Rare Disease Company in Germany.

SLC20A2
Specificity
100 %
Genes
25 %
AllNeuro panel.

By Centogene AG - the Rare Disease Company in Germany.

F2, F5, FMR1, HTT, HFE, MTHFR, TTR, UBE3A, VHL, PTEN, AARS2, ABHD12, ACACA, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1 , (...)

View the complete list with 1185 more genes
Specificity
1 %
Genes
25 %
Intellectual Disability NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

BRCA2, F5, FMR1, MTHFR, TTR, UBE3A, PTEN, MCCC1, MCCC2, AGL, ACAT1, GYS2, ARG1, ATP7A, AUH, BCS1L, ADSL, FBLN5, LRP5, COL1A2 , (...)

View the complete list with 372 more genes
Specificity
1 %
Genes
25 %
SLC20A2.

By Fulgent Genetics Fulgent Genetics in United States.

SLC20A2
Specificity
100 %
Genes
25 %
Ataxia Panel.

By Blueprint Genetics in Finland.

FMR1, ABHD12, TWNK, PRKCG, PAX6, INPP5E, OPA1, WFS1, CC2D2A, ELOVL4, TMEM67, ARL6, NPHP1, MKKS, CEP290, TTC8, TRIM32, POLG, NDUFS4, AFG3L2 , (...)

View the complete list with 137 more genes
Specificity
1 %
Genes
25 %
Basal ganglia calcification type 1.

By LifeLabs Genetics in Canada.

SLC20A2
Specificity
100 %
Genes
25 %

Alternate names

Basal Ganglia Calcification, Idiopathic, 1; Ibgc1 Is also known as striopallidodentate calcinosis, bilateral;bspdc, striopallidodentate calcinosis, autosomal dominant, adult-onset, cerebral calcification, nonarteriosclerotic, idiopathic, adult-onset, ferrocalcinosis, cerebrovascular, fahr disease, familial, formerly, basal ganglia calcification, idiopathic, 3, formerly;ibgc3, formerly;bspdc; cerebrovascular ferrocalcinosis; idiopathic basal ganglia calcification; pfbc; primary familial brain calcification.



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