Dermatology

Laryngo-onycho-cutaneous Syndrome

Feb 12, 2018 by in Dermatology Comments Off on Laryngo-onycho-cutaneous Syndrome

Laryngo-onycho-cutaneous (LOC) syndrome was reclassified as a subtype of junctional epidermolysis bullosa (JEB) based on clinical features similar to JEB and its association, in the majority of patients from the…

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Non-Herlitz Junctional Epidermolysis Bullosa

Feb 12, 2018 by in Dermatology Comments Off on Non-Herlitz Junctional Epidermolysis Bullosa

Non-Herlitz junctional epidermolysis bullosa (nH JEB) is characterized by generalized blisters that predominate in sites exposed to friction, trauma, or heat. Whereas infants and children with nH JEB often appear…

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Epidermolysis Bullosa with Pyloric Atresia

Feb 12, 2018 by in Dermatology Comments Off on Epidermolysis Bullosa with Pyloric Atresia

Epidermolysis bullosa (EB) with pyloric atresia (PA) is a rare form of EB. This article describes the clinical and pathologic features and molecular genetics of EB-PA, the mutations in the…

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Collagen XVII

Feb 12, 2018 by in Dermatology Comments Off on Collagen XVII

Collagen XVII has been identified as having a role in inherited junctional epidermolysis bullosa non-Herlitz (JEB-other, MIM #226650). The role of collagen XVII in both autoimmune and genetic blistering disorders…

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Herlitz Junctional Epidermolysis Bullosa

Feb 12, 2018 by in Dermatology Comments Off on Herlitz Junctional Epidermolysis Bullosa

Junctional epidermolysis bullosa type Herlitz (JEB-H) is the autosomal recessively inherited, more severe variant of “lucidolytic” JEB. Characterized by generalized, extensive mucocutaneous blistering at birth and early lethality, this devastating…

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Mutation Mechanisms

Feb 12, 2018 by in Dermatology Comments Off on Mutation Mechanisms

A mutation is an event that produces heritable changes in the DNA. There are many different types of mutations, including point mutations (changes that imply loss, duplication, or alterations of…

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Epidermolysis Bullosa Simplex

Feb 12, 2018 by in Dermatology Comments Off on Epidermolysis Bullosa Simplex

The prevalence of epidermolysis bullosa simplex (EBS) is estimated to be approximately 6 to 30 per 1 million live births. The disease is usually caused by missense mutations in KRT5…

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