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Epidermolysis bullosa simplex with anodontia/hypodontia

MONDO:0016514

Also known as: Gamborg-Nielsen syndrome, Kallin syndrome

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (680) Hereditary disease (176) Skin disorder (132) Epidermolysis bullosa (22) Human disease (14) Hereditary skin disorder (6) Epidermolysis bullosa simplex (5) Inherited epidermolysis bullosa (5) Vesiculobullous skin disease (3) Disease of genetic or genomic mechanism (2)

CBD oil may soothe itch in kids with rare skin disease

Symptom relief Completed

This study tested whether cannabidiol (CBD) can reduce severe itching in 10 children with a rare genetic skin condition called epidermolysis bullosa. The children took CBD syrup three times a day for a month. Researchers measured itch, pain, sleep, and quality of life before and …

Phase: PHASE2 • Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Symptom relief

Last updated Jun 27, 2026 09:10 UTC