Marfan’s Disease
Pathophysiology of Marfan’s disease
Marfan’s disease is
1) disease of connective tissue
2) marked by dilation of aorta and aortic dissection in a young person
Signs and Symptoms
1) tall stature with long lower torso
2) long limbs and digits
3) pectus carinatum (pigeon breast)
4) inguninal hernias
5) hypermobile joints
6) severe chest pain
7) lightheadedness
8) retinal detachment
9) myopia
10) bilateral subluxation of lines in outward and upward direction (ectopia lentis)
11) aortic regurgitation
12) mitral prolapse and “floppy” mitral valve
13) abnormal head (enlarged supraorbital ridges)
14) kyphosis/scoliosis
Characteristic Test Findings
Radiology
1) apical lung blebs on chest radiograph
Echocardiogram
2) enlarged aortic root
3) mitral valve prolapse and regurgitation
4) aortic dissection
Histology/Gross Pathology
fragmentation of elastic fibers in aortic media (cystic medial necrosis)
Associated Conditions
1) spontaneous pneumothorax
2) attention deficit disorder
Biochemistry
1) FBN1 gene codes for the extracellular glycoprotein fibrillin 1, a major component of microfibrils
2) if microfibril is abnormal, elastin cannot be correctly deposited on i
Inheritance/Epidemiology
1) automsomal dominant (75-85%) with some sporadic cases occurring
2) wide variation in clinical phenotype
3) occurs in 1/10,000 births
4) defect is usually a missense mutation occurring in the FBN1 gene (15q21.1)
Treament
1) ARB and ACE class drugs are being used early in the dis...
Source: Inside Surgery - Category: Surgeons Authors: Editor Tags: Pediatrics Surgpedia ectopia lentis FBN1 lens subluxation rfibrillin 1 Source Type: blogs
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