Epidermolysis bullosa simplex is one of a group of genetic conditions called epidermolysis bullosa that cause the skin to be very fragile and to blister easily. Epidermolysis bullosa (EB) is a group of genetic conditions that result in easy blistering of the skin and mucous membranes. Blisters occur with minor trauma or . Prevención de Ampollas. Como cargar al bebé: Evite levantar el bebé o niño por debajo de los brazos. En su lugar, ponga una mano debajo del trasero y la otra.

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A consensus approach to wound care in epidermolysis bullosa. Epidermolysis bullosa simplex Epidermolysis bullosa simplex usually becomes apparent at birth or during early epodermolisis. Epidermolysis bullosa EB is a genetic skin disorder characterized by skin tearing and blistering at the slightest touch. Accessed June 15, Two case reports with year follow-up. InfancyNeonatal ICD The presentation and severity of EB are affected by the specific genetic defects causing the disease, and can be difficult to classify.

Internal organs and bodily systems can also be seriously affected by the disease. Bullosaa Journal of clinical and aesthetic dermatology.

Parents’ indulgence, a common characteristic in cases like this in which an actual life-threatening condition is present, has contributed significantly to her poor oral status 4,8, This website is for informational purposes, always check with your physician before adopting any medical treatment.

Epidermolysis bullosa epixermolisis be diagnosed either by a skin punch biopsy at the edge of a wound with immunofluorescent mapping, or via blood sample and genetic testing. Retrieved 6 April Hence, the amount of resulting scarring and constrictures, especially in a very apprehensive patient with acute dental anxiety, is reduced 5.

According to the clinical interview, hemorrhagic blisters in the mouth had been detected since early infancy. The most common oral manifestations of EB are painful blisters affecting all the oral surfaces.

The aim of this article is to describe two dental clinical treatments of recessive dystrophic EB cases and their specific clinical manifestations. Case 2 A 5-year-old African-American boy was admitted to treatment, because of white spot lesions, at our institution.


After the contact with the patient’s physician, a panoramic radiograph was taken and a treatment plan was developed Figure 6. The frequency of milia, mild atrophic scarring, focal plantar hyperkeratosis and nail dystrophy is intermediate between that of localized EBS and EBS-DM see these termsand extracutaneous findings, other than occasional intraoral blistering, are rare.

But you can take steps to help prevent blisters and infection.

Oral-clinical findings and management of epidermolysis bullosa. The dystrophic forms of EB are characterized by deformities of the skin including coalescence of the fingers, blistering, scarring, nail changes and milia formation, and have either autosomal recessive or dominant inheritance 16, Mayo Clinic Marketplace Check out these best-sellers and special offers on books and newsletters from Mayo Clinic.

This occurs at different levels, depending on the subtype of EB. Unsourced or poorly sourced material may be challenged and removed.

This syndrome is rare within this disease, and characterized by blisters on the hands and feet, altered eimple coloring, and damage to the inner lining of areas such as the mouth, intestines, or eyes. These disorders are usually passed on by two carriers. Combined medical-dental treatment of an epidermolysis bullosa patient.

Epidermólisis Bullosa Simple by Maria Fernanda Marenco Salazar on Prezi

The disease gene may epideemolisis passed on from one parent who has the disease autosomal dominant inheritance. Epidermolysis bullosa EB comprises a group of genetically determined skin fragility disorders characterized by blistering of the skin and mucosa following mild mechanical trauma 18,20, For all other comments, please send your remarks via contact us.

Extraction of maxillary right first molar, first premolar, lateral incisor and central incisor, maxillary left central incisor, lateral incisor and first premolar, mandibular left first molar, mandibular right first and second premolars and first molar, and restorative treatment of second premolar, canine, mandibular left first premolar and mandibular right lateral incisor were recommended. EBA is a non-genetic autoimmune diseasecaused by the development of antibodies proteins that attack foreign substances against type VII collagen, an essential skin protein.

Types of Epidermolysis Bullosa

Some people don’t develop signs and symptoms until adolescence or early adulthood. Dental disease and caries related microflora in children with dystrophic epidermolysis bullosa. For infants, severe blistering can be life-threatening. Archived from the original on 22 December To avoid trauma to the fragile oral mucosa, precautions were adopted, including the use of gentle pressure during the surgeries and no suture usage.


Epidermolysis bullosa – Wikipedia

Microstomia, blister formation and the poor patient cooperation all together made the surgical procedures even more difficult and challenging. Erosions, blisters and eventually a tongue without papillae are observed in addition to ankyloglossia and microstomia 2,12,17,23, August 17, Modification: A person with an autosomal dominant disorder — in this case, the father — has a 50 percent chance of having an affected child with one mutated gene dominant gene and a 50 percent chance of having an unaffected child bullowa two normal genes recessive bulloda.

Daily wound care, pain management, and protective bandaging are the only options available for people with EB. We use cookies to ensure that we give you the best experience on our epidermoliais. Additional information Further information on this disease Classification s 2 Gene s 2 Clinical signs and symptoms Other website s 9.

There are four major types of EB based on the site of blister formations within the skin layers: The various types of epidermolysis bullosa are largely defined by which layer the blisters form in. EBS is the most common type of EB, accounting for 70 percent of cases. It’s not possible to prevent epidermolysis bullosa. Using Urgotul dressing for the bulloa of epidermolysis bullosa skin lesions.

Evite ropas con elasticos apretados, ziperes, y botones o broches asperos. In an autosomal dominant disorder, the mutated gene is a dominant gene located bulllosa one of the nonsex chromosomes autosomes. Sufferers of EB have compared the sores with third-degree burns.