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EB Dystrophic According to the Debra International Website: Dystrophic EB Some of the very earliest research on inherited EB was directed toward DEB. In 1969, Eisen postulated that excessive fibroblast collagenase activity was the underlying cause of subepidermal blister formation and dermal collagenolysis in patients with DEB. Subsequent in vitro studies in the 1970s by Lazarus and Bauer and co-workers suggested that this mechanism was correct. The possible pathogenicity of skin collagenase in RDEB was further supported by the intriguing observation by Bauer and colleagues in 1980 that the treatment of a series of RDEB patients with systemic phenytoin led both to a reduction in blister counts and to the reduced synthesis of collagenase by dermal fibroblasts from these patients. Interest in collagenase as a primary cause of RDEB waned by the late 1980s as data increasingly suggested type VII collagen as a more likely primary target. In 1992, Hovnanian and colleagues provided the final evidence against tissue collagenase being the underlying basis for RDEB by demonstrating, using molecular techniques, a lack of linkage between the collagenase gene and the RDEB phenotype.
In 1986, Heagerty, Eady, and co-workers demonstrated that RDEB skin basement membrane stained poorly or not at all when a monoclonal antibody (LH 7:2), subsequently proven by Leigh and others to react against type VII collagen, was used as an immunohistochemical probe. This finding proved to be the basis for the eventual identification of the molecular etiology of RDEB since one year previously Lunstrom and colleagues had shown that the anchoring fibril, a basement membrane-associated structure known for many years to be absent or reduced in number in RDEB skin, was composed of type VII collagen. These collective findings therefore suggested that type VII collagen might indeed he the target for genetic mutation in RDEB. In 1992, Rynnanen, Uitto, and colleagues demonstrated linkage of the type VII collagen gene to DDEB. Similar findings were reported in RDEB by Uitto, Christiano, and co-workers, beginning in 1993, followed by the mapping of specific mutations in the type VH collagen gene in numerous DDEB and RDEB kindreds. Collectively, these findings have convincingly demonstrated that the underlying molecular cause of all forms of DEB is the presence of mutations in the gene encoding for the anchoring fibril-specific protein, type VII collagen. EB Acquisita In 1981, Yaoita and colleagues demonstrated that skin from patients with EB acquisita contains in vivo-bound immunoglobulins in the lamina densa of the dermoepidermal junction, distinguishing them from those immunoreactants observed in another autoimmune. subepidermal, blistering disease, bullous pemphigoid. In the early 1980s, Gammon and co-workers showed that EB acquisita sera contained autoantibodies that bound to either or both the lamina densa and adjacent anchoring fibrils of normal human skin, and then devised an elegant in vitro model, termed the leukocyte attachment assay, to demonstrate the temporal relationship between the binding or. attachment of EB acquisita autoantibodies, complement, and functional leukocytes along the dermoepidermal junction and the subsequent development of microvesiculaton. In 1984, Woodley and colleagues identified in skin extracts two protein bands, having molecular weights of 290 and 145 kD, which reacted specifically with EB acquisita autoantibodies. In 1987, Woodley further showed that these autoantibodies recognize type VII collagen. In 1988, Gammon et al. showed that patients with EB acquisita were likely to have the HLA-DR2 histocompatability haplotype, adding further evidence to the role of immunogeneticity to this disease. Finally, Lapiere and co-workers in 1993 demonstrated that autoantibodies in EB acquisita sera recognize only limited epitopes in the type VII collagen molecule. According to the Debra U.S. Website: Dystrophic Epidermolysis Bullosa What Is The Cause Of Dystrophic EB? Through research it is now known that the genes that carry the instructions necessary to produce the proteins in the basement membrane zone of the skin, are faulty. This results in incorrectly formed anchoring fibrils, deeming them unable to perform their normal role as a 'stable interweave' between the dermal and epidermal layers of the skin. Mutation (a change in the genetic material) occurs within the collagen VII gene, which encodes the protein of the anchoring fibril. Anchoring fibrils hold together the two layers of skin. As a result, there is a lack of adherence and disruption of the skin when any friction or trauma occurs to an area. Where the two layers separate there is a blister. Blistering in the various types of dystrophic EB causes scarring. There are two major types of DEB:
How is Dominant Dystrophic Epidermolysis Bullosa Inherited? DDEB is an autosomal dominant condition. One parent of an affected person will usually also have the condition. It is possible for DDEB to appear 'sporadically' (to appear for the first time in a person who has no other affected family member). Anyone who has DDEB whether male or female, can pass the condition on to his or her children. Each time a pregnancy occurs, there is a 1 in 2 chance that the child will inherit DDEB. Electron microscopic evaluation reveals skin separation at the level of the sub lamina densa of the basement membrane zone, with normal or decreased number of anchoring fibrils. Mutations are noted in the genes encoding collagen VII either the gene from the mother or from the father. The change that results, decreases the functioning of the anchoring fibrils, but does not eliminate the anchoring fibrils Dominant Dystrophic Epidermolysis Bullosa : There is usually generalized blistering noted at birth. Blistering may be generalized or appear only on the hands, feet, elbows or knees: this is usually due to mechanical trauma. Rarely does scarring cause immobility and deformity of the hands and feet. Small cysts or milia are seen at sites of scarring. There may be mild involvement of the mucous membranes, nails may be thick, dystrophic or destroyed. Some affected by this form of EB may note the presence of small, firm flesh colored or white skin elevations that appear spontaneously on the trunk and extremeties of their body, that are called albopapuloid lesions.
How is Recessive Dystrophic Epidermolysis Bullosa Inherited? RDEB is an autosomal recessive inherited condition. This means both parents are carriers, yet they are unaffected. When each parent has a copy of the altered gene, there is a 1 in 4 chance or 25% that the child will be affected. Unfortunately, there is no test to detect carriers for RDEB. We are made aware that the parents are carriers after their child is born. Electron microscopic evaluation reveals skin separation at the level of the sub lamina densa, with absence of anchoring fibrils in RDEB-HS. There are reduced or occasionally abnormal appearing anchoring fibrils in RDEB-nHS. Mutations in RDEB are found in both the mother’s and the father’s gene encoding collagen VII. Recessive Dystrophic Epidermolysis Bullosa: Although in some cases this form of EB can be mild with generalized blistering, typically the recessive forms of EB tend to be more severe. Onset is usually at birth with areas of missing skin. Generalized blistering then scarring can occur on skin surfaces and mucous membranes. Scarring may limit range of motion of extremities. Fusion of fingers and toes and contractures cause deformity and loss of function. In some cases there is relatively mild blistering on hands, feet, elbows, and knees; these cases are very similar to dominant dystrophic EB. However, recessive dystrophic epidermolysis bullosa typically is characterized as follows: Blistering onset is at birth or soon afterwards. In some cases, nearly all skin surfaces and mucous membranes (from mouth to anus) are covered by blisters. Large areas may be devoid of skin. There is widespread scarring and deformity. Fingers and toes may become immobile. With recurrent scarring, fingers and/or toes may fuse together. Hands and arms may become fixed in a flexed position with resulting contractures. There is usually loss of the nails of the fingers and toes. Teeth may be malformed and delayed in appearing through the gums. Because routine dental care can raise blisters, many persons with RDEB have a higher than normal incidence of cavities. Blistering on the mucosal surfaces often cause scarring within the mouth and gastrointestinal tract. The ingestion of food may be limited due to microstomia (inability to fully open mouth due to scarring and contractures of the perioral region), painful swallowing, difficulty chewing, (due to poor dentition) esophageal webbing. In many cases chronic malnutrition, growth retardation and anemia may ensue. Involvement of the eyes can include eyelid inflammation with adhesions to the eyeball, as well as inflammation of the cornea or the conjunctiva (the mucous membrane covering the eyeball and the underside of the lids). RDEB inversa is a rare subtype of RDEB, blistering is noted on intertriginous (areas where skin rubs on skin i.e. axilla and groin) Lumbosacral areas may be affected as well. Common Manifestations of DEB: *Since EB varies in severity these manifestations may or may not be experienced by the individual affected.
Rare Manifestations of DEB:
Skin Cancers and Dystrophic Epidermolysis Bullosa It is important to note that skin cancers usually react differently in a patient with EB. The more severely affected individual (RDEB) appears to be more at risk for developing squamous cell carcinoma. These localized skin cell tumors have the ability to grow faster and spread to other areas of the body more rapidly then they would on a less compromised individual. Patients and caregivers need to examine skin carefully for any changes. It is important to perform self examinations of your skin at home. Many times it is helpful to have family members look at areas that are not often viewed by the affected individual, such as the back or upon the scalp. Mirrors can be helpful in detecting growths on the back of trunk and extremities when you are self examining. Any suspicious lesions, moles or markings should be evaluated by a dermatologist. Yearly full body exams are usually recommended, however, in some instances your dermatologist may modify the frequency of skin exams.
Changes in skin that warrant visit to physician for prompt evaluation include the following:
Generally biopsies are obtained to confirm the presence of skin cancer. However, if a biopsy is obtained from a suspicious growth and the results are negative, please continue to monitor the area. If the area is still not healing please notify your physician, it may be necessary to re-biopsy the area. For helpful hints on self examination please note the following web-site for the Skin Cancer Foundation http://www.skincancer.org/self_exam/spot_skin_cancer.html How is EB Treated? Because EB involves many systems of the body, parents and health professionals must take a 'team approach' , to the treatment of an EB patient. Intense and total patient care often must be provided, particularly for young and growing children. The severe forms of EB require hours of intensive nursing care that in many ways is similar to that given to burn patients. Much of this care is often provided by the parents; however, the education of all people who have contact with the patient is essential. These people may include the primary care physician (often a pediatrician), the dermatologist, the nurse, the pediatric dentist, the specialist in gastrointestinal (digestive) diseases, the dietitian or nutritionist, the plastic surgeon, the psychologist or social worker, and the genetic counselor, as well as teachers, relatives, baby sitters, and others. So far, research has not yet found a cure for epidermolysis bullosa or a treatment to completely control any form of EB. However, many complications can be lessened or avoided through early intervention. Many persons with milder forms have minimal symptoms and may require little or no treatment. In all cases, treatment of EB is directed towards the symptoms and is largely supportive. This care should focus on prevention of infection, protection of the skin against trauma, attention to nutritional deficiencies and dietary complications, minimization of deformities and contractures, and the need for psychological support for the entire family. According to the Telemedicine Website of Stanford University: Dystrophic: blistering below the lamina densa level AF1, AF2, LH7:2, L3d, np185, np32 (all mAb directed against type VII collagen) usually show absent IF staining in Hallopeau-Siemens recessive dystrophic EB, and reduced or absent staining in involved skin areas of most of the dominant subtypes. A large variety of mutations of the COL7A1 gene coding for type VII collagen has been demonstrated in a number of families with both dominant and recessive forms of dystrophic epidermolysis bullosa. No other genes have yet been reported to be affected in this group of diseases. A) Dystrophic EB- Cockayne-Touraine INHERITANCE: Autosomal Dominant CUTANEOUS FINDINGS:
EXTRACUTANEOUS INVOLVEMENT:
PATHOLOGIC FINDINGS:
B) Dystrophic EB- Minimus INHERITANCE: Autosomal Dominant CUTANEOUS FINDINGS:
EXTRACUTANEOUS FINDINGS: none PATHOLOGIC FINDINGS:
C) Dystrophic EB- Pretibial INHERITANCE: Autosomal Dominant CUTANEOUS FINDINGS:
EXTRACUTANEOUS FINDINGS:
PATHOLOGIC FINDINGS:
D) Dystrophic EB- Albopapuloidea (Pasini variant) INHERITANCE: Autosomal Dominant CUTANEOUS FINDINGS:
EXTRACUTANEOUS FINDINGS:
PATHOLOGIC FINDINGS:
E) Dystrophic EB- Hallopeau-Siemens (Gravis) INHERITANCE: Autosomal Recessive CUTANEOUS FINDINGS:
EXTRACUTANEOUS FINDINGS:
PATHOLOGIC FINDINGS:
F) Dystrophic EB- Inversa INHERITANCE: Autosomal Recessive CUTANEOUS FINDINGS:
NONCUTANEOUS FINDINGS:
PATHOLOGIC FINDINGS:
G) Dystrophic EB- Transient bullous dermolysis of the newborn INHERITANCE: Autosomal Dominant; Some may be Autosomal Recessive CUTANEOUS FINDINGS:
EXTRACUTANEOUS FINDINGS: none PATHOLOGIC FINDINGS:
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EB Info World was Created on 11/20/1997 - Background Ribbon Graphic by Dominic
Gionfriddo
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