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NA10695 DNA from LCL

Description:

MARFAN SYNDROME; MFS

Affected:

Yes

Sex:

Female

Age:

4 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • External Links

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Class Disorders of Connective Tissue, Muscle, and Bone
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
Race White
Family Member 6
Relation to Proband daughter
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Arachnodactyly; enlarged aortic root (>95%); pectus carinatum

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis
 
GENE MAPPING & DOSAGE STUDIES - Y CHROMOSOME PCR analysis of DNA from this cell culture gave a negative result with a primer for Yq11, DYS227.
 

Phenotypic Data

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Demographic Data
Relation to Proband daughter
Age at Sampling 4 YR
Sex Female
Racial Category White
 
Data Elements
Clinical Element Type: Marfan's Syndrome
  (Baseline)
Inheritance
Family history of Marfan Syndrome Yes  No  Unknown  
If yes, give relationship of affected family members  No Data
Growth
Length at birth in cm  No Data
Adult height in cm  No Data
Disproportionate tall stature Yes  No  Unknown  
Arm span to height ratio (give ratio)  No Data
Puberty-associated peak in growth velocity Yes  No  Unknown  
Head and Neck
Dolichocephaly Yes  No  Unknown  
Long, narrow face Yes  No  Unknown  
Malar hypoplasia Yes  No  Unknown  
Micrognathia Yes  No  Unknown  
Retrognathia Yes  No  Unknown  
Enophthalmos Yes  No  Unknown  
Ectopia lentis Yes  No  Unknown  
If yes, type:  No Data
Myopia Yes  No  Unknown  
If yes, type  No Data
Increased axial globe length Yes  No  Unknown  
Corneal flatness Yes  No  Unknown  
Retinal detachment Yes  No  Unknown  
Iris hypoplasia Yes  No  Unknown  
Early glaucoma Yes  No  Unknown  
Early cataracts Yes  No  Unknown  
Down-slanting palpebral fissures Yes  No  Unknown  
High-arched palate Yes  No  Unknown  
Narrow palate Yes  No  Unknown  
Dental Crowding (malocclusion) Yes  No  Unknown  
Cardiovascular
Aortic regurgitation Yes  No  Unknown  
Mitral regurgitation Yes  No  Unknown  
Mitral valve prolapse Yes  No  Unknown  
Congestive heart failure Yes  No  Unknown  
Tricuspid valve prolapse Yes  No  Unknown  
Premature calcification of mitral annulus Yes  No  Unknown  
Aortic root dilatation (ascending aorta) Yes  No  Unknown  
Aortic dissection (ascending aorta) Yes  No  Unknown  
Ascending aortic aneurysm Yes  No  Unknown  
If yes, give age at diagnosis (yrs)  No Data
Dilatation or dissection of the descending or abdominal aorta before age 50 Yes  No  Unknown  
Pulmonary artery dilatation Yes  No  Unknown  
Aortic root replacement Yes  No  Unknown  
If yes, give age at time of replacement (yrs)  No Data
Atrial septal defect Yes  No  Unknown  
Respiratory
Emphysema in most severe presentation Yes  No  Unknown  
Pneumothorax Yes  No  Unknown  
Pulmonary blebs Yes  No  Unknown  
Chest
Pectus excavatum Yes  No  Unknown  
If yes, type:  No Data
Pectus carinatum Yes   No  Unknown 
If yes, type:  No Data
Thoracic asymmetry Yes  No  Unknown  
Abdomen
Hernia Yes  No  Unknown  
If yes, give type(s):  No Data
Skeletal
Premature arthritis Yes  No  Unknown  
Scoliosis Yes  No  Unknown  
If yes, type:  No Data
Kyphoscoliosis Yes  No  Unknown  
Thoracic lordosis Yes  No  Unknown  
Spondylolisthesis Yes  No  Unknown  
Lumbosacral dural ectasia Yes  No  Unknown  
Protrusio acetabulae Yes  No  Unknown  
Long bone overgrowth (dolichostenomelia) Yes  No  Unknown  
Joint laxity (hypermobility) Yes  No  Unknown  
If yes, list affected joints  No Data
Limited elbow extension Yes  No  Unknown  
Joint contractures Yes  No  Unknown  
Genu recurvatum Yes  No  Unknown  
Arachnodactyly Yes   No  Unknown 
Pes planus Yes  No  Unknown  
Long, narrow feet Yes  No  Unknown  
Pes cavus Yes  No  Unknown  
Hammer toes Yes  No  Unknown  
Medial rotation of the medial malleolus Yes  No  Unknown  
Muscle
Decreased muscle mass Yes  No  Unknown  
Skin, Nails, Hair
Striae distensae Yes  No  Unknown  
Decreased subcutaneous fat Yes  No  Unknown  
Central Nervous System
Dural ectasia Yes  No  Unknown  
major CNS involvement Yes  No  Unknown  
Laboratory Abnormalities
Decreased fibrillin-1 immunostaining in the dermis Yes  No  Unknown  
Molecular Basis
Mutation in FBN1 gene Yes  No  Unknown  
If yes, give mutation  No Data
Remarks Arachnodactyly; enlarged aortic root (>95%); pectus carinatum

External Links

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dbSNP dbSNP ID: 11422
Gene Cards FBN1
NCBI GTR 154700 MARFAN SYNDROME; MFS
OMIM 154700 MARFAN SYNDROME; MFS
Omim Description MARFAN SYNDROME, TYPE I; MFS1
  MARFAN SYNDROME; MFS
Pricing
International/Commercial/For-profit:
$281.00USD
U.S. Academic/Non-profit/Government:
$139.00USD
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How to Order
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