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NA23095 DNA from LCL

Description:

MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
DYSTROPHIN; DMD

Affected:

Yes

Sex:

Male

Age:

No Data

  • Overview
  • Characterizations
  • Phenotypic Data
  • External Links

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Muscular Dystrophies
Class Congenital Muscle Diseases
Quantity 25 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
Family Member 1
Family History N
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Clinically affected; affected brother is GM23096; diagnosed at 2 years of age; frequent falls; walks without mobility devices; currently on daily corticosteroids; diagnosed with heart problem; on Enalapril; donor subject has a deletion of exons 35-43 in the DMD gene

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by LINE assay
 
Gene DMD
Chromosomal Location Xp21.2
Allelic Variant 1 deleted exons 35-43; DUCHENNE MUSCULAR DYSTROPHY
Identified Mutation EX35-43DEL

Phenotypic Data

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Demographic Data
Relation to Proband proband
Sex Male
 
Data Elements
Clinical Element Type: Duchenne Muscular Dystrophy
  (Baseline)
Diagnosis
Muscle Pain with increased activity or exercise  No
Age at Diagnosis (in years)  2
Age at first symptom or medical concern  3 YR
Relative with similar muscle disease  Yes
If yes, give their relationship(s) to you  No Data
Skeletal/Mobility
Scoliosis  No
Broken bones due to DMD  No
If yes, broke:  No Data
Delays in motor development was initially recognized  No
Toe Walking initially recognized  No
Enlarged calves initially recognized  No
Walking  Yes
If yes, type of walking device  No Data
Mobility device ie stroller, wheelchair  No
If yes, age at the start of use  No Data
Stand without aid  Yes
Sit without aid  Yes
Neurologic
Problem controlling behavior  No
Learning disability  No
Treatment
Use of corticosteroids  Yes
If yes, list those you are currently taking  DEFLAZACORT
What is the current dosage of medication(s)  DAILY
Use of alternative therapies  No
Type of breathing device used, if any  No Data
Taking heart medication  Yes
Tendon release surgery  No
If yes, give location at which surgery was performed  No Data
Laboratory Tests
Taken the Forced Vital Capacity (FVC%) test  No
Date of the most recent FVC Test  No Data
Percent value from the most recent FVC Test  No Data
Cardiomyopathy  Yes
Cardiac MRI  No
Echocardiogram  Yes
Holter monitor  No
Taken the Left Ventricular Fraction (LVEF) test  Yes
Percent value from the most recent LVEF Test  No Data
Taken the Left Ventricular Shortening Fraction (LVSF) test  Yes
Percent value from the most recent LVSF Test  No Data
Had muscle biopsy  No
Immunohistochemistry: N-terminus  No Data
Immunohistochemistry: C-terminus  No Data
Immunohistochemistry: Rod domain  No Data
Molecular Tests
Immunblot/Western blot: Quantity (%)  No Data
Immunblot/Western blot: Molecular size  No Data
Immunblot/Western blot: Dystrophic changes  No Data
Genetic test performed  Yes
If yes, list identified mutation  DEL OF EXONS 35-43
Testing method used  No Data
Remarks Clinically affected; affected brother is GM23096; diagnosed at 2 years of age; frequent falls; walks without mobility devices; currently on daily corticosteroids; diagnosed with heart problem; on Enalapril; donor subject has a deletion of exons 35-43 in the DMD gene

External Links

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Gene Cards DMD
Gene Ontology GO:0003779 actin binding
GO:0005200 structural constituent of cytoskeleton
GO:0005509 calcium ion binding
GO:0005856 cytoskeleton
GO:0006936 muscle contraction
GO:0007016 cytoskeletal anchoring
GO:0007517 muscle development
GO:0008270 zinc ion binding
GO:0016010 dystrophin-associated glycoprotein complex
NCBI Gene Gene ID:1756
NCBI GTR 300377 DYSTROPHIN; DMD
310200 MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
OMIM 300377 DYSTROPHIN; DMD
310200 MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
Omim Description APO-DYSTROPHIN 1, INCLUDED
  BMDDYSTROPHIN, INCLUDED; DMD, INCLUDED
  CARDIOMYOPATHY, X-LINKED DILATED, INCLUDED; XLCM, INCLUDED
  MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC PROGRESSIVE, DUCHENNE AND BECKERTYPES; DMD
Pricing
Commercial/For-profit:
$281.00USD
Academic/Non-profit/Government:
$139.00USD
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How to Order
  • Ordering Instructions
  • MTA / Assurance Form
  • Statement of Research Intent Form
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