Epidermolysis Bullosa Dystrophica

"Epidermolysis Bullosa Dystrophica" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in COLLAGEN TYPE VII, a major component fibrils of BASEMENT MEMBRANE and EPIDERMIS.

Descriptor ID	D016108
MeSH Number(s)	C16.131.831.493.160 C16.320.850.275.160 C17.300.200.367 C17.800.804.493.160 C17.800.827.275.160 C17.800.865.410.160
Concept/Terms	Epidermolysis Bullosa Dystrophica Epidermolysis Bullosa Dystrophica Bullosa Dystrophica, Epidermolysis Bullosa Dystrophicas, Epidermolysis Dystrophica, Epidermolysis Bullosa Dystrophicas, Epidermolysis Bullosa Epidermolysis Bullosa Dystrophicas Epidermolysis Bullosa, Dystrophic Dystrophic Epidermolysis Bullosa Bullosa, Dystrophic Epidermolysis Bullosas, Dystrophic Epidermolysis Dystrophic Epidermolysis Bullosas Epidermolysis Bullosas, Dystrophic Hallopeau-Siemens Disease Hallopeau-Siemens Disease Hallopeau Siemens Disease Epidermolysis Bullosa Dystrophica, Autosomal Recessive Dystrophic Epidermolysis Bullosa, Autosomal Recessive Epidermolysis Bullosa Dystrophica, Recessive Epidermolysis Bullosa Dystrophica, Hallopeau-Siemens Type Epidermolysis Bullosa Dystrophica, Hallopeau Siemens Type Cockayne-Touraine Disease Cockayne-Touraine Disease Cockayne Touraine Disease Cockayne-Touraine Type Epidermolysis Bullosa Cockayne Touraine Type Epidermolysis Bullosa Epidermolysis Bullosa Dystrophica, Dominant Epidermolysis Bullosa Dystrophica, Cockayne-Touraine Type Epidermolysis Bullosa Dystrophica, Cockayne Touraine Type

Below are MeSH descriptors whose meaning is more general than "Epidermolysis Bullosa Dystrophica".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Skin Abnormalities [C16.131.831]
Epidermolysis Bullosa [C16.131.831.493]
Epidermolysis Bullosa Dystrophica [C16.131.831.493.160]
Genetic Diseases, Inborn [C16.320]
Skin Diseases, Genetic [C16.320.850]
Epidermolysis Bullosa [C16.320.850.275]
Epidermolysis Bullosa Dystrophica [C16.320.850.275.160]
Skin and Connective Tissue Diseases [C17]
Connective Tissue Diseases [C17.300]
Collagen Diseases [C17.300.200]
Epidermolysis Bullosa Dystrophica [C17.300.200.367]
Skin Diseases [C17.800]
Skin Abnormalities [C17.800.804]
Epidermolysis Bullosa [C17.800.804.493]
Epidermolysis Bullosa Dystrophica [C17.800.804.493.160]
Skin Diseases, Genetic [C17.800.827]
Epidermolysis Bullosa [C17.800.827.275]
Epidermolysis Bullosa Dystrophica [C17.800.827.275.160]
Skin Diseases, Vesiculobullous [C17.800.865]
Epidermolysis Bullosa [C17.800.865.410]
Epidermolysis Bullosa Dystrophica [C17.800.865.410.160]

Below are MeSH descriptors whose meaning is related to "Epidermolysis Bullosa Dystrophica".

Below are MeSH descriptors whose meaning is more specific than "Epidermolysis Bullosa Dystrophica".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Epidermolysis Bullosa Dystrophica" by people in this website by year, and whether "Epidermolysis Bullosa Dystrophica" was a major or minor topic of these publications.

Bar chart showing 8 publications over 7 distinct years, with a maximum of 2 publications in 2025

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2009	1	0	1
2014	1	0	1
2017	1	0	1
2019	0	1	1
2021	1	0	1
2022	1	0	1
2025	2	0	2

Below are the most recent publications written about "Epidermolysis Bullosa Dystrophica" by people in Profiles.

Tang JY, Marinkovich MP, Wiss K, McCarthy D, Truesdale A, Chiou AS, Eid E, McIntyre JK, Bailey I, Furukawa LK, Gorell ES, Harris N, Khosla RK, Peter Lorenz H, Lu Y, Nazaroff J, Grachev ID, Moore AJ. Prademagene zamikeracel for recessive dystrophic epidermolysis bullosa wounds (VIITAL): a two-centre, randomised, open-label, intrapatient-controlled phase 3 trial. Lancet. 2025 Jul 12; 406(10499):163-173.

View in: PubMed
Pathmarajah P, Eid E, Nazaroff J, So J, Mittal V, Harris N, Li S, Lucky AW, Gorell ES, Peoples KG, Pope E, Lara-Corrales I, Paller AS, Wiss K, Perman MJ, Eichenfield LF, Levy ML, Morel KD, Garc?a-Romero MT, McCuaig CC, Saber M, Marinkovich MP, Oro A, Bruckner AL, Tang JY. Functional genotype classification groups distinguish disease severity in recessive dystrophic epidermolysis bullosa. Br J Dermatol. 2025 Apr 28; 192(5):917-925.

View in: PubMed
Garza-Mayers AC, Su KA, Wiss K. Improved erythema and decreased blister formation in dominant dystrophic epidermolysis bullosa following treatment with pulsed dye laser. Pediatr Dermatol. 2022 Nov; 39(6):1005-1006.

View in: PubMed
Phillips GS, Huang A, Augsburger BD, Kaplan L, Peoples K, Bruckner AL, Khuu P, Tang JY, Lara-Corrales I, Pope E, Wiss K, Levin LE, Morel KD, Hook KP, Paller AS, Eichenfield LF, McCuaig CC, Powell J, Castelo-Soccio L, Levy ML, Price HN, Schachner LA, Browning JC, Jahnke M, Shwayder T, Bayliss S, Lucky AW, Glick SA. A retrospective analysis of diagnostic testing in a large North American cohort of patients with epidermolysis bullosa. J Am Acad Dermatol. 2022 05; 86(5):1063-1071.

View in: PubMed
Evan-Browning E, Rork J, O'Donnell P, Elaba Z, Deng A, Wiss K. Verruciform xanthoma in recessive dystrophic epidermolysis bullosa and keratitis-ichthyosis-deafness syndrome: Report of two cases and a review of the literature. Pediatr Dermatol. 2020 Jan; 37(1):176-179.

View in: PubMed
Li AW, Prindaville B, Bateman ST, Gibson TE, Wiss K. Inpatient management of children with recessive dystrophic epidermolysis bullosa: A review. Pediatr Dermatol. 2017 Nov; 34(6):647-655.

View in: PubMed
Snadecki H, Criscione V, Jaquith A, Hay B, Deng A, Wiss K. Dystrophic epidermolysis bullosa associated with amniotic band syndrome. Pediatr Dermatol. 2014 Mar-Apr; 31(2):212-6.

View in: PubMed
Fleming KF, Wu JJ, Dyson SW, Dadras SS, Metz BJ. Denuded congenital lesions: recessive dystrophic epidermolysis bullosa. Dermatol Online J. 2009 Apr 15; 15(4):4.

View in: PubMed

People

Explore

Similar Concepts

Top Journals