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Juvenile hyaline fibromatosis

ORPHA:2028Clinical subtypeAutosomal recessiveChildhood

Ассоциированные гены (1)

ANTXR2
ANTXR cell adhesion molecule 2
Disease-causing germline mutation(s) in
OMIM: 608041

Фенотипы (16)

Очень частый (80–99%)6
HP:0000271Abnormality of the face
HP:0000929Abnormal skull morphology
HP:0000940Abnormal diaphysis morphology
HP:0001482Subcutaneous nodule
HP:0001595Abnormality of the hair
HP:0200034Papule
Частый (30–79%)3
HP:0001522Death in infancy
HP:0008065Aplasia/Hypoplasia of the skin
HP:0200042Skin ulcer
Периодический (5–29%)7
HP:0000169Gingival fibromatosis
HP:0000212Gingival overgrowth
HP:0001387Joint stiffness
HP:0002797Osteolysis
HP:0003202Skeletal muscle atrophy
HP:0005876Progressive flexion contractures
HP:0011024Abnormality of the gastrointestinal tract

Эпидемиология (2)

Cases/families
Worldwide
Point prevalence
<1 / 1 000 000
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы