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Greenberg dysplasia

ORPHA:1426DiseaseAutosomal recessiveAntenatal, Neonatal

Ассоциированные гены (1)

LBR
lamin B receptor
Disease-causing germline mutation(s) in
OMIM: 600024

Фенотипы (18)

Очень частый (80–99%)12
HP:0000926Platyspondyly
HP:0001004Lymphedema
HP:0001156Brachydactyly
HP:0001881Abnormal leukocyte morphology
HP:0002983Micromelia
HP:0003312Abnormal form of the vertebral bodies
HP:0006619Anterior rib punctate calcifications
HP:0008890Severe short-limb dwarfism
HP:0008905Rhizomelia
HP:0009106Abnormal pelvis bone ossification
HP:0011849Abnormal bone ossification
HP:0100569Abnormally ossified vertebrae
Частый (30–79%)6
HP:0000347Micrognathia
HP:0000774Narrow chest
HP:0001362Skull defect
HP:0004331Decreased skull ossification
HP:0011800Midface retrusion
HP:0100602Preeclampsia

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