Ehlers-Danlos Syndrome

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Original Editors - Corey Vogt from Bellarmine University's Pathophysiology of Complex Patient Problems project.

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Definition/Description

Ehlers-Danlos syndrome is a hereditary collagen disorder characterized by articular hypermobility, dermal hyperelasticity, and widespread tissue fragility (The Merck Manual).  Individuals with EDS demonstrate defects in the body's connective tissues, manifesting as altered strength, elasticity, integrity, and healing properties of the tissues.  The severity of the syndrome varies greatly depending upon the specific mutation with each type demonstrating integumentary and/or joint hypermobility or laxity.

Ehlers Danlos Syndrome has been reported with an initial discover date and description dating back to the fourth century BC.  The first clinical description of EDS is credited to Tschernogobow in 1892.  However, the name and recognition of the syndrome is credited to Edward Ehlers, a Danish dermatologist, and Henri-Alexandre Danlos, a French physician, who wrote separate reports in 1901 and 1908 respectively.  The two physicians were able to collaborate in providing a description of the pertinent features of the condition as well as accurately identify the associated phenotypes.

In 1997-1998, six discernable phenotypes for EDS were identified (classic, hypermobility, vascular, kyphoscoliosis, arthorchalasia, and dermatosparaxis) by Beighton et. al.  These identifiable forms of EDS are currently recognized by the medical advisory board of the Ehlers-Danlos National Foundation and used in the clinical setting for proper diagnosis. 

Prevalence

Combined prevalence of all subtypes of EDS is about 1 per 5,000.  Hypermobility and classic subtypes are the most common with prevalencs of 1 per 10,000-15,000 and 1 per 20,000-40,000 respectively.  EDS demonstrates equal prevalence amongst males and females of all racial and ethnic backgrounds (Ehlers Danlos National Foundation, Steiner RD - emedicine, Levy HP - Gene Reviews, U.S. National Library of Medicine).

 

 

Associated Co-morbidities

Many different medical conditions/disease states occur in individuals with EDS.  Examples of co-morbidities include:

• Gastroesophageal reflux
• Gastritis
• Irritable Bowel Sydrome
• Autonomic Dysfunction (neurally mediated hypotension, postural orthostatic tachycardia syndrome, paroxysmal supraventricular tachycardia)
• Aortic root dilatation
• Mitral valve prolapse

Medications

Analgesics

• Acetaminophen
• Tramadol
• Lidocaine
• Tricyclic antidepressants
• Opioids

NSAIDS (ibuprofen, naproxen, etc)

• Ibuprofen, naproxen, etc
• Cox-2 Inhibitors

Muscle relaxants

Glucosamine and Chondroitin

Diagnostic Tests/Lab Tests/Lab Values

Clinical Examination and a detailed family history have proven to be the most effective means of accurately diagnosing EDS

Laboratory studies can be utilized as supporting evidence to confirm the diagnosis of specific subtypes of EDS. 

Biochemical Studies can be used to analyze the make-up of collagen molecules in cultured skin fibroblasts and detect alterations to support a diagnosis of EDS:

• Type IV EDS - Vascular
• Type VIIA and VIIB EDS- Arthrochalasia
• Type VIIC - Dermatosparaxis

Molecular testing utilizing DNA analysis can be used in diagnosis of EDS:

• Type IV - Vascular
• Type VII - Arthrochalasia/Dermatosparaxis

Urinary Analyte Assay can be used in diagnosis of EDS:

• Type VI - Kyphoscoliotic

CT scanning, MRI scanning, ultrasonography, and angiography are useful in diagnosing Type IV (Vascular) EDS with reports suggesting the presence of arterial aneurysms, arterial dissections, arterial ectasias, and arterial occlusions.

Ultrastructural examination of collagen fibrils has been utilized as an assistive tool for diagnosis of Type I/II (Classical) EDS and Type VIIA/Type VIIB ( Arthrochalasia) EDS.

Skin Biopsy using histopathologic analysis has yet to be proven as beneficial in the diagnostic process of EDS.

Causes

EDS is classified as an inherited connective tissue disease.  Three patterns of inheritance have been linked with the various subtypes of EDS: autosomal dominant, autosomal recessive, and X-linked, the rarest form.  The exact source of genetic mutation responsible for the disease state is unknown.  However, mutations in ADAMTS2, COL1A1, COL1A2, COL3A1, COL5A1, COL5A2, PLOD1, and TNXB genes have been linked to causation of EDS. 

COL1A1, COL1A2, COL3A1, COL5A1, COL5A2 encode the manufacture of proteins that are responsible for multiple types of collagen

ADAMTS2, PLOD1, and TNXB encode the manufacture of proteins that interact with or process collagen

 

EDS presents with 100% penetrance, but expression varies greatly amongst the many types

Systemic Involvement

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Medical Management (current best evidence)

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Physical Therapy Management (current best evidence)

Resistance training

• low resistance
• high repetitions

Myofascial release

• pain relief
• muscle spasms

Modalties

• hot/cold pack
• massage
• ultrasound
• electrical stimulation
• acupunture
• acupressure

Alternative/Holistic Management (current best evidence)

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Differential Diagnosis

Marfans Syndrome

Loeys-Dietz Syndrome

Stickler Syndrome

Williams Syndrome

Aarskog-Scott Syndrome

Fragile X Syndrome

Achondroplasia/hypochondroplasia

Osteogenesis Imperfecta

Aneuploidies

• Down Syndrome
• Turner Syndrome
• Klinefelter Syndrome

Case Reports

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Resources

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Recent Related Research (from Pubmed)

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References

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