Anagram & Information om | Engelska ordet BULLOSA

Exempel på hur man kan använda BULLOSA i en mening

• The American Belgian Draft has a high incidence of junctional epidermolysis bullosa, an inherited genetic disorder that affects newborn foals, often resulting in death.
• Epidermolysis bullosa (EB) is a group of rare medical conditions that result in easy blistering of the skin and mucous membranes.
• It is found largely in the upper spinous layer of epidermal keratinocytes and mutations in the gene encoding this protein have been associated with ichthyosis bullosa of Siemens.
• Mutations in the genes for these keratins are associated with epidermolysis bullosa simplex and dermatopathia pigmentosa reticularis, both of which are autosomal dominant mutations.
• Esophageal webs are associated with bullous diseases (such as epidermolysis bullosa, pemphigus, and bullous pemphigoid), with graft versus host disease involving the esophagus, and with celiac disease.
• Missense mutations can render the resulting protein nonfunctional, and such mutations are responsible for human diseases such as Epidermolysis bullosa, sickle-cell disease, SOD1 mediated ALS, and a substantial number of cancers.
• Four of the hospitals (Boston, Galveston, Cincinnati, and Sacramento) provide care for children with burns, as well as treating a variety of skin conditions such as epidermolysis bullosa and toxic epidermal necrolysis.
• These glycoproteins are imperative to the maintenance and vitality of tissues; defective laminins can cause muscles to form improperly, leading to a form of muscular dystrophy, lethal skin blistering disease (junctional epidermolysis bullosa), and/or defects of the kidney filter (nephrotic syndrome).
• It is used to treat two types of epidermolysis bullosa, dystrophic and junctional, targeting partial-thickness skin wounds.
• Jonathan "Jonny" Kennedy (4 November 1966 – 26 September 2003) was a British man who had a rare inherited condition known as dystrophic epidermolysis bullosa (EB or DEB).
• Epidermolysis bullosa acquisita, a chronic subepidermal blistering disease associated with autoimmunity.
• Jonathan Pitre (2000–2018), Canadian sufferer, and awareness champion, of the rare condition recessive dystrophic epidermolysis bullosa (RDEB).
• The condition may be caused by epidermolysis bullosa, specific teratogens, or intrauterine infections, or it may be caused by chromosomal abnormalities, ectodermal dysplasias, or other malformation syndromes.
• It is used off-label to treat various dermatological conditions, including psychogenic itch, drug-induced hyperhidrosis (excessive sweating), and prevention of blister formation for some people with epidermolysis bullosa simplex.
• Epidermolysis bullosa simplex (EBS) is a disorder resulting from mutations in the genes encoding keratin 5 or keratin 14.
• Photopheresis has also been successful in treating epidermolysis bullosa acquisita when all other treatments have been ineffective.
• These garments have also been effective in treating multiple sclerosis, peripheral neuropathy, epidermolysis bullosa, spina bifida, and cerebral palsy, by providing controlled cooling to the body.
• Inserting this mutant keratin into transgenic mice caused heavy epidermal blistering; analysis showed this blistering to be nearly identical to the dermatological disorder epidermolysis bullosa simplex.
• Epidermolysis bullosa simplex (EBS) is an inherited skin blistering disorder associated with mutations in either K5 or K14.
• Junctional epidermolysis bullosa (JEB) is an inherited disorder that is also known as red foot disease or hairless foal syndrome.

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