Mitis junctional epidermolysis bullosa

Mitis junctional epidermolysis bullosa
Mitis junctional epidermolysis bullosa
Classification and external resources
OMIM 226650

Mitis junctional epidermolysis bullosa (also known as "Nonlethal junctional epidermolysis bullosa") is a skin condition characterized by scalp and nail lesions, also associated with periorificial nonhealing erosions.[1]:599 Mitis junctional epidermolysis bullosa is most commonly seem in children between the ages of 4 and 10 years old.[1]:600

See also

References

  1. ^ a b Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0071380760.


EB
and related
EBS (EBS-K, EBS-WC, EBS-DM, EBS-OG, EBS-MD, EBS-MP)
JEB (JEB-H, Mitis, Generalized atrophic, JEB-PA)
DEB (DDEB, RDEB)
related: Costello syndrome · Kindler syndrome · Laryngoonychocutaneous syndrome · Skin fragility syndrome ·
Hyperkeratosis/
keratinopathy
Other

cadherin (EEM syndrome· immune system (Hereditary lymphedema, Mastocytosis/Urticaria pigmentosa· Hailey–Hailey

see also Template:Congenital malformations and deformations of skin appendages, Template:Phakomatoses, Template:Pigmentation disorders, Template:DNA replication and repair-deficiency disorder
Developmental
anomalies

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