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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El vestuario secundario debe de ser cambiado diariamente, igual que las heridas deben de ser evaluadas diariamente. Epidermolysis bullosa A five-year-old boy with epidermolysis bullosa Specialty Dermatology Symptoms Painful skin blisters [1] [2] Complications Esophageal narrowingsquamous cell skin canceramputations [3] [4] Usual onset At birth [4] Duration Often lifelong [4] Types Epidermolysis bullosa simplexdystrophic epidermolysis bullosajunctional epidermolysis zimpleKindler syndrome [1] Causes Genetic [1] Diagnostic method Skin biopsygenetic testing [5] Epidemrolisis diagnosis Bullous pemphigoidpemphigus vulgarisfriction blisters, insect bites [4] Treatment Wound carepain control, controlling infections, nutritional support [1] Frequency c.

Developmental defects of enamel in human with hereditary epidermolysis bullosa. Uso prolongado de Bactroban ha sido asociado con el desarrollo de infecciones de Estafilococo Resistente.

The patient has been under control of oral health since he was 2 years old. Although the clinical manifestations suggested EB diagnosis in both byllosa presented hereby, confirmation was granted by histopathologic study conducted at Lauro de Souza Lima Hospital, Bauru, SP, Brazil.

It’s the most common and epidremolisis severe type. To have an autosomal recessive disorder, you inherit two mutated genes, one from each parent. After the contact with the patient’s physician, a panoramic radiograph was taken and a treatment plan was developed Figure 6.


EB affects both genders and every racial and ethnic background equally.

Acta Dermatovenerol Alp Panonica Adrait. In our cases, the presence of polymorphic lesions involving the oral mucous membrane and tongue were present. This website is for informational purposes, always check with your physician before adopting any medical treatment. Retrieved 6 April What is Epidermolysis Bullosa EB?

Genetic counseling Epifermolisis is autosomal dominant and sporadic cases are frequent. Mayo Clinic does not endorse companies or products. The disorder occurs in every racial and ethnic group and affects both sexes.

Epidermolysis bullosa – Wikipedia

An examination of skin blisters will show antibodies deposited in the basement membrane between the epidermis smiple dermis. In individuals with epldermolisis skin, there are protein anchors between these two layers that prevent them from moving independently from one another shearing. Epidermolysis Bullosa ep-i-der-mo-lie-sis bu-low-suhor EB, is a rare genetic connective tissue disorder that affects 1 out of every 20, births in the United States approximately children a year are born with EB.

This content does not have an English version. The dental treatment of the patient of Case 1 was not very simple, whereas the patient of Case 2 required only preventive measures.

Surgical management of hand contractures and pseudosyndactyly in dystrophic epidermolysis bullosa. Retrieved 11 October It has also been designed to evaluate the response to new therapies for epidrrmolisis treatment of EB. Congenital malformations and deformations of skin appendagesTemplate: Gene therapy in combination with tissue engineering to treat epidermolysis bullosa.


Types of Epidermolysis Bullosa

As a result, severe forms of the disease may be fatal. Pediatr Clin North Am. Within each type, there are many subtypes. The most common oral manifestations of EB are painful blisters affecting all the oral surfaces. A consensus approach to wound care in epidermolysis bullosa. It was presented at the International Investigative Dermatology congress in Edinburgh in and a paper-based version was published in the Journal of the American Academy of Dermatology in Approximately , people are affected epiidermolisis and no definitive treatments have yet been developed 8,7.

The use of corticoids, vitamin E and immunosuppressive drugs have also been suggested for the treatment of EB 1,2,14, Blistering tendency usually worsens in summertime or in warm weather. Only comments written in English can be processed. Dental caries risk in hereditary epidermolysis bullosa.

Epidermolysis bullosa – Symptoms and causes – Mayo Clinic

Journal of the American Academy of Dermatology. Sign up to receive the latest in research, news, and events! The restorative treatment using glass ionomer cement was accomplished within 5 weeks.

Paller A, eipdermolisis al. Parents’ indulgence, a common characteristic in cases like this in which epkdermolisis actual life-threatening condition is present, has contributed significantly to her poor oral status 4,8, Dystrophic epidermolysis bullosa is an inherited variant affecting the skin and other organs. There was no family history of EB.