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Platyspondylic dysplasia, Torrance type

ORPHA:85166Malformation syndromeAutosomal dominantAntenatal, Infancy, Neonatal

Ассоциированные гены (1)

COL2A1
collagen type II alpha 1 chain
Disease-causing germline mutation(s) in
OMIM: 120140

Фенотипы (25)

Очень частый (80–99%)15
HP:0000774Narrow chest
HP:0000926Platyspondyly
HP:0001191Abnormal carpal morphology
HP:0001773Short foot
HP:0002652Skeletal dysplasia
HP:0002983Micromelia
HP:0003021Metaphyseal cupping
HP:0003090Hypoplasia of the capital femoral epiphysis
HP:0003270Abdominal distention
HP:0004279Short palm
HP:0006487Bowing of the long bones
HP:0008839Hypoplastic pelvis
HP:0008873Disproportionate short-limb short stature
HP:0009882Short distal phalanx of finger
HP:0010306Short thorax
Частый (30–79%)9
HP:0000272Malar flattening
HP:0000369Low-set ears
HP:0000882Hypoplastic scapulae
HP:0001561Polyhydramnios
HP:0001789Hydrops fetalis
HP:0002089Pulmonary hypoplasia
HP:0002970Genu varum
HP:0005280Depressed nasal bridge
HP:0011220Prominent forehead
Периодический (5–29%)1
HP:0000175Cleft palate

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