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Progressive symmetric erythrokeratodermia

ORPHA:316DiseaseAutosomal dominantInfancy, Neonatal

Ассоциированные гены (4)

TRPM4
transient receptor potential cation channel subfamily M member 4
Disease-causing germline mutation(s) (gain of function) in
OMIM: 606936
KRT83
keratin 83
Disease-causing germline mutation(s) (loss of function) in
OMIM: 602765
KDSR
3-ketodihydrosphingosine reductase
Disease-causing germline mutation(s) (loss of function) in
OMIM: 136440
LORICRIN
loricrin cornified envelope precursor protein
Candidate gene tested in
OMIM: 152445

Фенотипы (3)

Очень частый (80–99%)3
HP:0000982Palmoplantar keratoderma
HP:0010783Erythema
HP:0200035Skin plaque

Эпидемиология (1)

Point prevalence
Unknown
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы