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GM07726 Fibroblast

Description:

MARFAN SYNDROME; MFS

Affected:

Yes

Sex:

Female

Age:

12 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • External Links
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Class Disorders of Connective Tissue, Muscle, and Bone
Cell Type Fibroblast
Transformant Untransformed
Race Black/African American
Family Member 1
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Similarly affected mother; long face; high arched palate; genu valgum; mild scoliosis; tall; wide arm span; decreased U/L segment ratio; no chest or eye abnormalities; mitral valve prolapse; arachnodactyly; see GM07727A Lymphoid

Characterizations

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Passage Frozen 2
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis
 

Phenotypic Data

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Demographic Data
Relation to Proband proband
Age at Sampling 12 YR
Sex Female
Racial Category Black/African American
 
Data Elements
Clinical Element Type: Marfan's Syndrome
  (Baseline)
Inheritance
Family history of Marfan Syndrome Yes  No  Unknown  
Growth
Disproportionate tall stature Yes  No  Unknown  
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  
Myopia Yes  No  Unknown  
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  
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  
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  
Pectus carinatum Yes  No  Unknown  
Thoracic asymmetry Yes  No  Unknown  
Abdomen
Hernia Yes  No  Unknown  
Skeletal
Premature arthritis Yes  No  Unknown  
Scoliosis Yes   No  Unknown 
If yes, type:  Moderate
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  
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  No Data
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  
Remarks Similarly affected mother; long face; high arched palate; genu valgum; mild scoliosis; tall; wide arm span; decreased U/L segment ratio; no chest or eye abnormalities; mitral valve prolapse; arachnodactyly; see GM07727A Lymphoid

External Links

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dbSNP dbSNP ID: 17283
Gene Cards FBN1
NCBI GTR 154700 MARFAN SYNDROME; MFS
OMIM 154700 MARFAN SYNDROME; MFS
Omim Description MARFAN SYNDROME, TYPE I; MFS1
  MARFAN SYNDROME; MFS

Culture Protocols

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Passage Frozen 2
Split Ratio 1:4
Temperature 37 C
Percent CO2 5%
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not inactivated
Substrate None specified
Subcultivation Method trypsin-EDTA
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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