Epidermolysis bullosa simplex due to plakophilin deficiency

MONDO:0011472

Epidermolysis bullosa simplex due to plakophilin deficiency (EBS-PD) is a suprabasal subtype of epidermolysis bullosa simplex (EBS) characterized by generalized superficial erosions and less commonly blistering.

Also known as: McGrath syndrome, ectodermal dysplasia-skin fragility syndrome, Mcgrath syndrome, ectodermal dysplasia - skin fragility syndrome, ectodermal dysplasia skin fragility syndrome, ectodermal dysplasia/skin fragility syndrome

8 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Syndromic disease (24) Epidermolysis bullosa (21) Human disease (14) Hereditary skin disorder (5) Inherited epidermolysis bullosa (5) Epidermolysis bullosa simplex (4) Ectodermal dysplasia syndrome (3)

Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 1 Completed 2

Skin deep: european study probes the hidden emotional toll of skin diseases

Knowledge-focused Not yet recruiting

This study looks at how people with skin conditions (like eczema, psoriasis, or skin cancer) manage stress, feel lonely, and bounce back from challenges. Researchers will compare 375 adults with and without skin disease across 15 European countries using questionnaires. The goal …

Phase: NA • Sponsor: University Hospital, Brest • Aim: Knowledge-focused

Last updated Jun 27, 2026 13:06 UTC

Epidermolysis bullosa simplex due to plakophilin deficiency

Broader categories

Skin deep: european study probes the hidden emotional toll of skin diseases