Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 1
1991 1
1992 1
2003 1
2006 1
2010 1
2022 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

7 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Acral dystrophic epidermolysis bullosa"
Page 1
Case report: bullous pemphigoid development underlies dystrophic epidermolysis bullosa disease worsening.
Di Zenzo G, Floriddia G, Rossi S, Mariotti F, Primerano A, Condorelli AG, Didona B, Castiglia D. Di Zenzo G, et al. Front Immunol. 2022 Jul 29;13:929286. doi: 10.3389/fimmu.2022.929286. eCollection 2022. Front Immunol. 2022. PMID: 35967298 Free PMC article.
Autoimmune response to cutaneous basement membrane components superimposed on a genetic skin fragility disease, hereditary epidermolysis bullosa (EB), has been described, but its effects on disease course remain unclear. We report a 69-year-old individual wit …
Autoimmune response to cutaneous basement membrane components superimposed on a genetic skin fragility disease, hereditary epidermolysis …
Dystrophic epidermolysis bullosa complicated by cutaneous squamous cell carcinoma and pulmonary and renal amyloidosis.
Csikós M, Orosz Z, Bottlik G, Szöcs H, Szalai Z, Rozgonyi Z, Hársing J, Török E, Bruckner-Tuderman L, Horváth A, Kárpáti S. Csikós M, et al. Clin Exp Dermatol. 2003 Mar;28(2):163-6. doi: 10.1046/j.1365-2230.2003.01185.x. Clin Exp Dermatol. 2003. PMID: 12653705
A 25-year-old woman with Hallopeau-Siemens recessive dystrophic epidermolysis bullosa had generalized blistering, scarring and milia since birth. ...The possibility of secondary pulmonary amyloidosis should be considered in severe dystrophic epiderm …
A 25-year-old woman with Hallopeau-Siemens recessive dystrophic epidermolysis bullosa had generalized blistering, scarr …
Cancer complicating chronic ulcerative and scarifying mucocutaneous disorders.
Kaplan RP. Kaplan RP. Adv Dermatol. 1987;2:19-46. Adv Dermatol. 1987. PMID: 3079255 Review.
The other extreme on the temperature scale can less often result in enough permanent acral damage that poor wound healing may eventually result in cancer, usually SCC. ...In acrodermatis chronica atrophicans, a condition not often seen in the United States, the involved sk …
The other extreme on the temperature scale can less often result in enough permanent acral damage that poor wound healing may eventua …
Epidermolysis bullosa simplex (Dowling-Meara). A clinicopathological review.
McGrath JA, Ishida-Yamamoto A, Tidman MJ, Heagerty AH, Schofield OM, Eady RA. McGrath JA, et al. Br J Dermatol. 1992 May;126(5):421-30. doi: 10.1111/j.1365-2133.1992.tb11813.x. Br J Dermatol. 1992. PMID: 1610681
The clinicopathological features of 22 cases of the Dowling-Meara form of epidermolysis bullosa simplex (DM-EBS) (11 males, 11 females; aged 5 days-46 years) were reviewed using data collected over a 10-year period. ...We conclude that DM-EBS is a distinct, and prob …
The clinicopathological features of 22 cases of the Dowling-Meara form of epidermolysis bullosa simplex (DM-EBS) (11 males, 11 …
The first COL7A1 mutation survey in a large Spanish dystrophic epidermolysis bullosa cohort: c.6527insC disclosed as an unusually recurrent mutation.
Escámez MJ, García M, Cuadrado-Corrales N, Llames SG, Charlesworth A, De Luca N, Illera N, Sánchez-Jimeno C, Holguín A, Duarte B, Trujillo-Tiebas MJ, Vicario JL, Santiago JL, Hernández-Martín A, Torrelo A, Castiglia D, Ayuso C, Larcher F, Jorcano JL, Meana A, Meneguzzi G, Zambruno G, Del Rio M. Escámez MJ, et al. Br J Dermatol. 2010 Jul;163(1):155-61. doi: 10.1111/j.1365-2133.2010.09713.x. Epub 2010 Feb 22. Br J Dermatol. 2010. PMID: 20184583
BACKGROUND: Dystrophic epidermolysis bullosa (DEB) is a genodermatosis caused by mutations in COL7A1. ...Specifically, 27 displayed the severe generalized subtype, eight the other generalized subtype and six a localized phenotype (two pretibial, three acra …
BACKGROUND: Dystrophic epidermolysis bullosa (DEB) is a genodermatosis caused by mutations in COL7A1. ...Specifically, …
Metastatic squamous cell carcinoma resembling angiosarcoma complicating dystrophic epidermolysis bullosa.
McGrath JA, Schofield OM, Mayou BJ, McKee PH, Eady RA. McGrath JA, et al. Dermatologica. 1991;182(4):235-8. doi: 10.1159/000247803. Dermatologica. 1991. PMID: 1884860
We report a patient with generalized recessive dystrophic epidermolysis bullosa (RDEB) who developed 3 squamous cell carcinomas. The tumours appeared simultaneously at acral sites on both upper limbs and were poorly differentiated. Despite surgery and …
We report a patient with generalized recessive dystrophic epidermolysis bullosa (RDEB) who developed 3 squamous cell ca …
Novel KIND1 gene mutation in Kindler syndrome with severe gastrointestinal tract involvement.
Sadler E, Klausegger A, Muss W, Deinsberger U, Pohla-Gubo G, Laimer M, Lanschuetzer C, Bauer JW, Hintner H. Sadler E, et al. Arch Dermatol. 2006 Dec;142(12):1619-24. doi: 10.1001/archderm.142.12.1619. Arch Dermatol. 2006. PMID: 17178989
BACKGROUND: Kindler syndrome (online Mendelian Inheritance in Man No. 173650) is an autosomal recessive genodermatosis characterized by acral trauma-induced blistering that improves with age and by progressive poikiloderma in later life. ...
BACKGROUND: Kindler syndrome (online Mendelian Inheritance in Man No. 173650) is an autosomal recessive genodermatosis characterized by a …