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Localized epidermolysis bullosa simplex

ORPHA:79400DiseaseAutosomal dominantChildhood

Ассоциированные гены (2)

KRT14
keratin 14
Disease-causing germline mutation(s) in
OMIM: 148066
KRT5
keratin 5
Disease-causing germline mutation(s) in
OMIM: 148040

Фенотипы (23)

Очень частый (80–99%)7
HP:0000989Pruritus
HP:0003341Junctional split
HP:0007446Palmoplantar blistering
HP:0007497Focal friction-related palmoplantar hyperkeratosis
HP:0007585Skin fragility with non-scarring blistering
HP:0008066Abnormal blistering of the skin
HP:0025238Foot pain
Частый (30–79%)5
HP:0002046Heat intolerance
HP:0003401Paresthesia
HP:0003489Acute episodes of neuropathic symptoms
HP:0012513Upper limb pain
HP:0200035Skin plaque
Периодический (5–29%)5
HP:0000975Hyperhidrosis
HP:0007556Plantar hyperkeratosis
HP:0010765Palmar hyperkeratosis
HP:0031446Erosion of oral mucosa
HP:0200041Skin erosion
Очень редкий (1–4%)5
HP:0001056Milia
HP:0001075Atrophic scars
HP:0008404Nail dystrophy
HP:0030350Erythematous papule
HP:0200097Oral mucosal blisters
Исключён (0%)1
HP:0009123Mixed hypo- and hyperpigmentation of the skin

Эпидемиология (1)

Point prevalence
1-9 / 1 000 000
Europe

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы