Mette Sommerlund
Overview
Explore the profile of Mette Sommerlund including associated specialties, affiliations and a list of published articles.
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84
Citations
298
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Recent Articles
1.
Svendsen S, Mose K, Simonsen A, Sommerlund M, Johansen J, Mortz C
Ugeskr Laeger
. 2025 Jan;
186(51).
PMID: 39749627
Contact dermatitis is a common skin condition in children caused by environmental exposure to irritants or allergens. Manifestation of common endogenous eczemas, e.g. atopic dermatitis, causes differential diagnostic challenges. The...
2.
Gram S, Brusgaard K, Lei U, Sommerlund M, Vinding G, Sleire S, et al.
JAMA Dermatol
. 2024 Dec;
161(2):157-166.
PMID: 39630431
Importance: Palmoplantar keratoderma poses diagnostic challenges due to its clinical and genetic heterogeneity, and knowledge on the value of systematic genetic testing on clinically well-described patient cohorts is sparse. Objective:...
3.
Herlin L, Schmidt S, Mogensen T, Sommerlund M
Orphanet J Rare Dis
. 2024 Dec;
19(1):454.
PMID: 39623400
Background: Incontinentia pigmenti (IP) is an X-linked dominant multisystemic disorder caused by pathogenic variants in the IKBKG gene. Population-based research into the epidemiology of IP is lacking. Methods: This nationwide...
4.
Blechingberg J, Terkelsen T, Jensen U, Ronholt K, Sommerlund M, Vinter H, et al.
Am J Med Genet A
. 2024 Nov;
197(3):e63933.
PMID: 39523677
Hailey-Hailey disease (OMIM#169600) is an autosomal dominantly inherited genodermatosis characterized by erosions in the flexural areas of the body. Hailey-Hailey disease is caused by variants in ATP2C1, but for ~10%...
5.
Graversen L, Sommerlund M, Kruse C, Gjorup H, Gregersen P, Jensen U, et al.
Eur J Med Genet
. 2024 Oct;
72:104982.
PMID: 39476951
Hypohidrotic Ectodermal Dysplasia is a syndrome with hypotrichosis, hypohidrosis, and hypodontia as the main symptoms. The prevalence is estimated to one in 5000-10,000 persons. In 10-15% the disease is caused...
6.
Andersen S, Herlin L, Schmidt S, Sommerlund M
JAMA Dermatol
. 2024 Oct;
160(12):1364-1366.
PMID: 39441584
No abstract available.
7.
Norreslet L, Ingham A, Agner T, Olesen C, Bregnhoj A, Sommerlund M, et al.
J Eur Acad Dermatol Venereol
. 2024 Oct;
PMID: 39360671
Background: More than 50% of patients with hand eczema (HE) are colonized with Staphylococcus aureus. Comprehensive knowledge of the skin microbiome and its changes in patients with HE may provide...
8.
Herlin L, Herlin M, Vinter H, Blechingberg J, Andersen B, Kruse C, et al.
Pediatr Dermatol
. 2024 Sep;
41(6):1106-1113.
PMID: 39256944
Background: Focal dermal hypoplasia (FDH), also known as Goltz syndrome, is a rare ectodermal dysplasia that primarily affects the skin, skeleton, and eyes. It is an X-linked dominant disorder, predominantly...
9.
Geilswijk M, Genuardi M, Woodward E, Nightingale K, Huber J, Madsen M, et al.
Eur J Hum Genet
. 2024 Jul;
32(12):1542-1550.
PMID: 39085584
Birt-Hogg-Dubé syndrome (BHD syndrome) is an autosomal dominant multisystem disorder with variable expression due to pathogenic constitutional variants in the FLCN gene. Patients with BHD syndrome are predisposed to benign...
10.