Arteriovenous Malformations Of The Brain

Clinical Features

Phenotypes and symptoms related to Arteriovenous Malformations Of The Brain

  • Seizures
  • Pain
  • Headache
  • Back pain
  • Abnormality of the cerebral vasculature
  • Visceral angiomatosis
  • Peripheral arteriovenous fistula
  • Cerebral arteriovenous malformation

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

Arteriovenous Malformations Of The Brain Is also known as cerebral arteriovenous malformations, bavm.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Arteriovenous Malformations Of The Brain Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Crohn Disease.

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NOD2, IL6
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50 %
Genes
50 %
IL6.

By Fulgent Genetics Fulgent Genetics (United States).

IL6
Specificity
100 %
Genes
50 %
OmniSeq Comprehensive.

By OmniSeq, Inc. (United States).

RHEB, BCL9, ROS1, RPS6KB1, SF3B1, FOXL2, BRAF, BRCA1, BRCA2, SMARCB1, SMO, SOX2, SPOP, SRC, BTK, STAT3, STK11, HNF1A, TERT, TIAF1 , (...)

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Specificity
2 %
Genes
100 %
Inflammatory Bowel Disease (IBD) and Related Disorders , Panel Massive Sequencing (NGS) 46 Genes.

By Reference Laboratory Genetics (Spain).

SH2D1A, STXBP2, TERC, TERT, TGFB1, TINF2, CD40LG, WAS, WIPF1, CARD9, IL17F, IL23R, ADAM17, ATG16L1, CTLA4, WRAP53, CYBA, CYBB, DKC1, IRGM , (...)

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Specificity
3 %
Genes
50 %
KRAS Sequence Analysis.

By Baylor Miraca Genetics Laboratories (United States).

KRAS
Specificity
100 %
Genes
50 %
KRAS Sequence Analysis (Familial Mutation/Variant Analysis).

By Baylor Miraca Genetics Laboratories (United States).

KRAS
Specificity
100 %
Genes
50 %
KRAS Sequence Analysis (Prenatal Diagnosis).

By Baylor Miraca Genetics Laboratories (United States).

KRAS
Specificity
100 %
Genes
50 %
PreSeek Non-invasive Prenatal Gene Sequencing Screen.

By Baylor Miraca Genetics Laboratories (United States).

RIT1, BRAF, SMC1A, SOS1, SOS2, CDKL5, SYNGAP1, TSC1, TSC2, HDAC8, NSD1, CBL, SHOC2, CHD7, COL1A2, SMC3, NIPBL, FGFR2, FGFR3, HRAS , (...)

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Specificity
4 %
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Sources and references

You can check the following sources for additional information.

ORPHANET MESH OMIM Rare Disease Search Engine

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