Ehlers-Danlos syndrome

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Ehlers-Danlos Syndrome
Classification and external resources
ICD-10 Q79.6
ICD-9 756.83
MedlinePlus 001468
eMedicine derm/696  ped/654
MeSH D004535

Ehlers-Danlos Syndrome (EDS) (also known as "Cutis hyperelastica"[1]) is a group of rare genetic disorders affecting humans caused by a defect in collagen synthesis. Depending on the individual mutation, the severity of the syndrome can vary from mild to life-threatening. There is no known cure. Treatment is supportive.

The syndrome is named after two doctors, Edward Ehlers of Denmark, and Henri-Alexandre Danlos of France, who identified it at the turn of the 20th century. [2]


[edit] Symptoms

Individual with EDS displaying hypermobile joints. Individual with EDS displaying hypermobile joints.
Individual with EDS displaying hypermobile joints.

Symptoms vary widely based on which type of EDS the patient has. In each case, however, the symptoms are ultimately due to faulty or reduced amounts of collagen. For example, in the most common type of EDS, Hypermobility Type, symptoms often include unstable, flexible joints with a painful tendency to dislocate and subluxate. This is due to ligaments which are overly stretchable because they are lacking proper collagen (the molecule that provides strength to ligaments). The so-called Classic EDS Type features skin that forms cigarette-paper-like scars – another type of collagen is usually responsible for lending strength to skin and scars. One of the rarest, and the most serious type of EDS, Vascular EDS, can result in premature death via vascular (blood vessel) and organ rupture [3] – again, another type of collagen is necessary to give strength to the walls of blood vessels and the walls of hollow organs (such as the colon). See table below for a more extensive list of symptoms for each type of EDS. There is some cross-over or similarity of symptoms among the various types. For example, many of the types feature velvety or hyperextensible skin. In addition, persons with Hypermobility Type often have very stretchy ligaments (leading to frequent subluxations/dislocations) while those with Vascular Type have ligaments that rupture. Because it is often undiagnosed, some instances of Ehlers-Danlos syndrome have been mischaracterized as child abuse.[4]

[edit] Classification

In the past, there were more than 10 recognized types of Ehlers-Danlos syndrome. In 1997, researchers proposed a simpler classification that reduced the number of major types to six and gave them descriptive names.[5] These six major types are listed here. Other types of the condition may exist, but they have been reported only in single families or are not well characterized. Except for hypermobility, the specific mutations involved have been identified and they can be precisely identified by genetic testing; this is valuable due to a great deal of variation in individual presentation of symptoms which may confuse classification of individuals on purely symptomatic basis. In order of prevalence in the population, they are:

Name Number Description OMIM Gene(s)
Hypermobility type 3 Affects 1 in 10,000 to 15,000 and is caused by an autosomal dominant mechanism. Mutations in either of two separate genes (which are also involved in Vascular EDS and Tenascin-X deficiency EDS, respectively) may lead to this variant; it is the only type of EDS that cannot be diagnosed through skin / tissue samples but is rather diagnosed through use of clinical observations. Symptoms can include easy bruising, velvety-smooth skin, low bone density, and loose, unstable joints. Joint dislocations and subluxations are common. Degenerative joint disease can occur; the pain associated with this condition is a serious complication. Functional bowel disorders, neurally mediated hypotension or postural orthostatic tachycardia syndrome, and dental crowding is common in individuals with this variant. Some individuals have mitral valve prolapse, which creates an increased risk for infective endocarditis during surgery, particularly dental surgery, as well as possibly progressing to a life-threatening degree of severity of the prognosis of mitral valve prolapse. 130020 COL3A1, TNXB
Classical types 1 and 2 Affects approximately 2 to 5 in 100,000 people. In addition to the joint and cardiac effects noted above for hypermobility, this variant is characterized by soft, highly elastic, velvety skin which may tear, bruise, or scar easily and/or be slow to heal, and which has a tendency to develop benign fatty growths as well as benign fibrous growths on pressure areas. Pregnancy can be life-threatening in this variant. It affects type-V collagen, as well as type I. 130000, 130010 COL5A1, COL5A2, COL1A1
Vascular type 4 Is an autosomal dominant defect in the type-III collagen synthesis; affecting approximately 1 in 100,000 people. It is clinically serious, and past studies have placed life expectancy at around 48 years. However, that number is likely skewed based on the fact that the disease is (as are all EDS types) vastly underdiagnosed, leading to a misleading proportion of people diagnosed being those diagnosed upon death. Increased awareness among physicians (and the public) will help make this number more accurate and bring down the overall number of premature deaths. Hypermobility is most apparent in the fingers or toes, but the delicate skin noted above is joined by fragile blood vessel walls and organ membranes, with a tendency to rupture or develop aneurysms. Patients typically have thin, pale, translucent skin (veins can usually be seen on chest); Arterial/intestinal/uterine fragility or rupture; extensive bruising; some patients express the characteristic facial appearance (large eyes, small chin, thin nose and lips, lobeless ears); low weight and average or short stature. Due to possibility of uterine rupture, pregnancy can be life-threatening in people with this variant. 130050 COL3A1
Kyphoscoliosis type 6 Is an autosomal recessive defect due to deficiency of an enzyme called lysyl hydroxylase; it is very rare, with fewer than 60 cases reported. Symptoms include progressive scoliosis, progressive severe weakness of muscles, and fragile sclera. 225400, 229200 PLOD1
Arthrochalasis types 7A and 7B Is also very rare, with about 30 cases reported. This variant may result in very loose and unstable joints, including the hips, which may lead to early and/or severe osteoarthritis and fractures, and stretchy, fragile skin. It affects type-I collagen. 130060 COL1A1, COL1A2
Dermatosparaxis type 7C Also very rare, with about 10 cases reported. This variant combines the loose and unstable joints with extremely fragile skin which loses elasticity. 225410 ADAMTS2

While the above symptomatology is clean and defined, the disease itself rarely obeys these neat categorizations. Cross-over symptoms for all types are prevalent and lead to under-diagnosis or mis-diagnosis. No patient should assume or rely on the "fact" they have a certain type of EDS when cross-over symptoms are evident and can be life-threatening.

"The large number of distinct types of the Ehlers-Danlos syndrome that have already been identified indicates great heterogeneity, but clearly that heterogeneity is not exhausted by the present classification." [1] Examples of types of related syndromes other than those above reported in the medical literature include:

[edit] Genetics

Mutations in the following can cause Ehlers-Danlos syndrome:

Mutations in these genes usually alter the structure, production, or processing of collagen or proteins that interact with collagen. Collagen provides structure and strength to connective tissue throughout the body. A defect in collagen can weaken connective tissue in the skin, bones, blood vessels, and organs, resulting in the features of the disorder.

Inheritance patterns depend on the type of Ehlers-Danlos syndrome. Most forms of the condition are inherited in an autosomal dominant pattern, which means only one of the two copies of the gene in question must be altered to cause the disorder. The minority are inherited in an autosomal recessive pattern, which means both copies of the gene must be altered for a person to be affected by the condition. Please refer to the summary for each type of Ehlers-Danlos syndrome for a discussion of its inheritance pattern.

[edit] Epidemiology

Ehlers-Danlos Syndrome is an inherited disorder estimated to occur in about 1 in 5000 births worldwide. Ehlers Danlos affects both males and females of all racial and ethnic backgrounds. Initially, prevalence estimates have previously ranged from 1 in 250,000 to 1 in 500,000 people, but these estimates were soon found to be vastly inaccurate as the disorder received further study and medical professionals became more adept at accurately diagnosing EDS. The prevalence of the six types differs dramatically. The most commonly occurring type is the hypermobility type, followed by the classical type. The other types of EDS are very rare. For example, fewer than 10 infants and children with the dermatosparaxis type have been described worldwide.

[edit] EDS-like symptoms in animals

Ehlers-Danlos-like syndromes have been shown to be hereditary in Himalayan cats, some domestic shorthair cats and in certain breeds of cattle. It is seen as a sporadic condition in domestic dogs.

[edit] See also

[edit] References

  1. ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. Page 512. ISBN 0721629210.
  2. ^ "Uncovered: How U.S. Health System Can Fail Even the Insured --- A Woman Endures 16-Month Odyssey To Get a Diagnosis", John Carreyrou, Wall Street Journal, November 16, 2007
  3. ^ Lawrence EJ (2005). "The clinical presentation of Ehlers-Danlos syndrome". Adv Neonatal Care 5 (6): 301–14. doi:10.1016/j.adnc.2005.09.006. PMID 16338669. 
  4. ^ The Press Enterprise, Redlands mother stung by untrue suspicions presses for accountability in child abuse inquiries, 2008-04-03
  5. ^ Beighton P, De Paepe A, Steinmann B, Tsipouras P, Wenstrup RJ (1998). "Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK)". Am J Med Genet 77 (1): 31–7. doi:10.1002/(SICI)1096-8628(19980428)77:1<31::AID-AJMG8>3.0.CO;2-O. PMID 9557891. 

[edit] External links

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