Transient bullous dermolysis of the newborn
Transient bullous dermolysis of the newborn (TBDN) is a skin condition that presents in newborns. It is characterized by blister formation secondary to even mild trauma.[1]:558
| Transient bullous dermolysis of the newborn | |
|---|---|
| Specialty | Dermatology |
A subtype of dystrophic epidermolysis bullosa, it is rare, usually inherited condition that presents with characteristic blisters at birth which resolve between six months and one year of age.[2]
Blisters may cover the entire body including the mouth, and as they heal, they may leave some mild scarring. In addition, nail changes may occur which can persist to adulthood.[2]
It is associated with COL7A1.[3]
The condition was described by Ken Hashimoto in 1985.[4][5]
See also
- Skin lesion
References
- James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
- "Transient bullous dermolysis of the newborn | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 11 August 2018.
- Hammami-Hauasli N, Raghunath M, Küster W, Bruckner-Tuderman L (December 1998). "Transient bullous dermolysis of the newborn associated with compound heterozygosity for recessive and dominant COL7A1 mutations". J. Invest. Dermatol. 111 (6): 1214–9. doi:10.1046/j.1523-1747.1998.00394.x. PMID 9856844.
- John Thorne Crissey; Lawrence C. Parish; Karl Holubar (2013). Historical Atlas of Dermatology and Dermatologists. CRC Press. p. 179. ISBN 978-1-84214-100-7.
- Murase, K; Kanoh, H; Ishii, N; Hashimoto, T; Nakano, H; Sawamura, D; Seishima, M (2011). "Bullous Dermolysis of the Newborn and Dystrophic Epidermolysis Bullosa Pruriginosa within the Same Family: Two Phenotypes Associated with a COL7A1 Mutation". Acta Dermato Venereologica. 91 (6): 730–731. doi:10.2340/00015555-1154. ISSN 0001-5555. PMID 21629976.
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