Medicine:Epidermolysis bullosa simplex

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Epidermolysis bullosa simplex
HandsEBS.JPG
Epidermolysis bullosa simplex

Epidermolysis bullosa simplex (EBS) is a disorder resulting from mutations in the genes encoding keratin 5 or keratin 14.[1]:598[2]

Epidermolysis bullosa simplex (EBS) is one of the major forms of epidermolysis bullosa, a group of genetic conditions that cause the skin to be very fragile and to blister easily.[3] Blister formation of EBS occurs at the dermal-epidermal junction.[4]

Signs and symptoms

Cause

Epidermolysis bullosa simplex is caused by genetic mutations that prevent the proper formation of protein structures in the skin’s epidermis. This results in skin that blisters easily, from even minor insults.  The affected genes, KRT5 and the KRT14, which are responsible for the creation of keratin 5 and keratin 14 proteins respectively, are tied to the four major types of epidermolysis bullosa simplex. However, a small number of epidermolysis bullosa simplex patients do not have mutations in their KRT5 and KRT14 genes.  Mutations in the PLEC gene are also being researched, specifically in the gene’s role in the Ogna form of epidermolysis bullosa simplex.  The PLEC gene is responsible for the formation of plectin, another skin protein that attaches the epidermis to the skin’s deeper layers.[5]

Diagnosis

Classification

Epidermolysis bullosa simplex may be divided into multiple types:

Type Locus & Gene OMIM
Epidermolysis bullosa simplex with migratory circinate erythema 12q13 (KRT5) Online Mendelian Inheritance in Man (OMIM) 609352
Epidermolysis bullosa simplex with mottled pigmentation.
Associated with a recurrent mutation in KRT14.[6]:557[7][8]
 12q13 (KRT5) Online Mendelian Inheritance in Man (OMIM) 131960
Epidermolysis bullosa simplex, autosomal recessive 17q12-q21 (KRT14) Online Mendelian Inheritance in Man (OMIM) 601001
Generalized epidermolysis bullosa simplex
Also known as "Koebner variant of generalized epidermolysis bullosa simplex", presents at birth to early infancy with a predilection for the hands, feet, and extremities, and palmar-plantar hyperkeratosis and erosions may be present.[1]:598[6]:556
 17q12-q21 (KRT5), 12q13 (KRT14) Online Mendelian Inheritance in Man (OMIM) 131900
Localized epidermolysis bullosa simplex
Also known as "Weber–Cockayne syndrome"[8]:460 and "Weber–Cockayne variant of generalized epidermolysis bullosa simplex", is characterized by onset in childhood or later in life, and is the most common variant of epidermolysis bullosa simplex.[1]:598[6]:557
 17q12-q21 (KRT5), 17q11-qter, 12q13 (KRT14) Online Mendelian Inheritance in Man (OMIM) 131800
Epidermolysis bullosa herpetiformis
Also known as "Dowling-Meara epidermolysis bullosa simplex", presents at birth with a generalized distribution, often with oral mucosa involvement and variable lesions in infancy.[1]:598[6]:557
 17q12-q21 (KRT5), 12q13 (KRT14) Online Mendelian Inheritance in Man (OMIM) 131760
Epidermolysis bullosa simplex with muscular dystrophy
A rare clinical entity, and is the only epidermolytic epidermolysis bullosa described that is not caused by a keratin mutation, presenting as a generalized intraepidermal blistering similar to the Koebner variant of generalized epidermolysis bullosa simplex, but also associated with adult onset muscular dystrophy.[1]:598[6]:557[8]
 8q24 (PLEC1) Online Mendelian Inheritance in Man (OMIM) 226670
Epidermolysis bullosa simplex with pyloric atresia 8q24 (PLEC1) Online Mendelian Inheritance in Man (OMIM) 612138
Epidermolysis bullosa simplex of Ogna
Has onset in infancy, presenting with seasonal blistering on acral areas during summer months.[1]:598[6]:557[8]
 8q24 (PLEC1) Online Mendelian Inheritance in Man (OMIM) 131950

Management

  • No cure for EB
  • Treat symptoms
  • Protect skin, stop blister formation, promote healing
  • Prevent complications
  • Necessary treatment: use oral and topical steroid for healing and prevent complication
  • Maintain cool environment, avoid overheating and decreases friction

See also

References

  1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN:0-07-138076-0.
  2. ↑ Bardhan, Ajoy; Bruckner-Tuderman, Leena; Chapple, Iain L. C.; Fine, Jo-David; Harper, Natasha; Has, Cristina; Magin, Thomas M.; Marinkovich, M. Peter et al. (2020-09-24). "Epidermolysis bullosa" (in en). Nature Reviews Disease Primers 6 (1): 78. doi:10.1038/s41572-020-0210-0. ISSN 2056-676X. PMID 32973163. https://www.nature.com/articles/s41572-020-0210-0. 
  3. ↑ "Epidermolysis bullosa simplex - About the Disease - Genetic and Rare Diseases Information Center" (in en). https://rarediseases.info.nih.gov/diseases/10752/epidermolysis-bullosa-simplex. 
  4. ↑ So, Jodi Y.; Teng, Joyce (1993), Adam, Margaret P.; Everman, David B.; Mirzaa, Ghayda M. et al., eds., "Epidermolysis Bullosa Simplex", GeneReviews® (Seattle (WA): University of Washington, Seattle), PMID 20301543, http://www.ncbi.nlm.nih.gov/books/NBK1369/, retrieved 2022-11-01 
  5. ↑ "Epidermolysis bullosa simplex: MedlinePlus Genetics" (in en). https://medlineplus.gov/genetics/condition/epidermolysis-bullosa-simplex/. 
  6. ↑ 6.0 6.1 6.2 6.3 6.4 6.5 James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN:0-7216-2921-0.
  7. ↑ Harel, A, et al. "Epidermolysis Bullosa Simplex with Mottled Pigmentation Resulting from a Recurrent Mutation in KRT14." Journal of Investigative Dermatology. (2006) 126, 1654–1657. doi:10.1038/sj.jid.5700296; published online 6 April 2006. [1]
  8. ↑ 8.0 8.1 8.2 8.3 Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1. 

Further reading

External links

Classification
External resources



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