ND35822

Coriell Institute for Medical Research

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ND35822 DNA from LCL

Description:

AVM-UNRUPTURED

Affected:

Yes

Gender:

Female

Age:

11 YR (At Sampling)

Overview
Phenotypic Data
External Links

Overview

Repository

NINDS Repository

Subcollection

Cerebrovascular Disease

Quantity

20 µg

Quantitation Method

Please see our FAQ

Biopsy Source

Peripheral vein

Cell Type

B-Lymphocyte

Tissue Type

Blood

Transformant

Epstein-Barr Virus

Sample Source

DNA from LCL

Race

White

Ethnicity

Not Hispanic/Latino

Country of Origin

USA

Family History

Species

Homo sapiens

Common Name

Human

Phenotypic Data

Demographic Data

Relation to Proband

No Data

Age at Sampling

11 YR

Gender

Female

Age of Onset(If not a control)

11 YR

Age at Diagnosis(If not a control)

11 YR

Hispanic or Latino/Not Hispanic or Latino

Not Hispanic/Latino

Racial Category

White

Country

USA

Diagnosed By

No Data

Data Elements

Clinical Element Type: Cerebrovascular Disease

(Baseline)

Longitudinal Data

Is this data Longitudinal (Follow-Up) Data?

yes no

Smoking History

smoking history

never former smoker current smoker

years smoking

No Data

Family History

Family history of Cerebrovascular Disease

present absent Unknown

Family History of Aneurysm

present absent Unknown

Aneurysm Location of affected Family Member

No Data

Specific diagnosis

Cerebrovascular diagnosis

silent cerebral infarction
transient ischemic attack
unruptured intracranial aneurysm
symptomatic ischemic stroke
symptomatic intracerebral hemorrhage
aneurysmal subarachnoid hemorrhage
vascular cognitive impairment
arteriovenous malformations (AVM)
other
Unaffected primary blood relative of proband
Cerebral Cavernous Malformation (CCM)
Hereditary Hemorrhagic Telangiectasia (HHT)

Prior Medical History

Pre-existing history of dementia

Present Absent

Pre-hemorrhage history of ischemic stroke

Present Absent Not Applicable

TOAST criteria

ischemic stroke subtype based on TOAST

not applicable

AVM subtype criteria

AVM type

unruptured ruptured not applicable

Spetzler-Martin score

Size

<30mm 30-60mm >60mm

AVM Location

Eloquent Non-eloquent

Venous drainage

Superficial Deep Both

Drainage Location

cortical
subcortical/deep
posterior fossa

Confirmation of diagnosis

did a neurologist confirm the cerebrovascular diagnosis

yes no

Medical History

hypertension

yes no

diabetes mellitus

yes no

atrial fibrillation

yes no

myocardial infarction

yes no

Other risk factors

yes no

Genetic Data of Subject

Mutation/s in subject's DNA (if present, describe)

present absent unknown

Medical History

Hypertension treated with medication

yes no

Blood pressure (at time of blood draw)

No Data

Other diagnosis

Parkinson's disease

yes no

Alzheimer's disease

yes no

Epilepsy

yes no

Amyotrophic lateral sclerosis

yes no

Dementia

yes no

Other Neurological Diagnosis(es)

yes no

Optional data

State Examination (MMSE) score

No Data

Neurological examination

No Data

Handedness

Right Left Ambidextrous

Montreal Cognitive Assessment(MoCA) score

No Data

External Links

NCBI GTR

108010 ARTERIOVENOUS MALFORMATIONS OF THE BRAIN

OMIM

108010 ARTERIOVENOUS MALFORMATIONS OF THE BRAIN

Omim Description

ARTERIOVENOUS MALFORMATIONS OF THE BRAIN

CEREBRAL ARTERIOVENOUS MALFORMATIONS

Culture Protocols

Split Ratio (Frequency)

1:4 (4 Days)

Temperature

37 C

Percent CO2

Percent O2

AMBIENT

Medium

Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent

Serum

15% fetal bovine serum Not Inactivated

Substrate

None specified

Subcultivation Method

dilution - add fresh medium

Supplement

Pricing

Commercial and Non-U.S.:

$0.00USD

U.S. Academic or
Non-profit:

$0.00USD

NINDS Repository Submitter (past or current) and/or Current NINDS Grantee

$0.00USD

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How to Order

Ordering Instructions
MTA / Assurance Form
Statement of Research Intent Form