← Назад

Tricho-dento-osseous syndrome

ORPHA:3352Malformation syndromeAutosomal dominantChildhood

Ассоциированные гены (1)

DLX3
distal-less homeobox 3
Disease-causing germline mutation(s) (loss of function) in
OMIM: 600525

Фенотипы (16)

Частый (30–79%)14
HP:0000264Abnormality of the mastoid
HP:0000268Dolichocephaly
HP:0000679Taurodontia
HP:0000687Widely spaced teeth
HP:0000691Microdontia
HP:0001597Abnormality of the nail
HP:0001808Fragile nails
HP:0002007Frontal bossing
HP:0006285Enamel hypomineralization
HP:0009722Dental enamel pits
HP:0011001Increased bone mineral density
HP:0011362Abnormal hair quantity
HP:0030312Obliteration of the calvarial diploe
HP:0030758Periapical tooth abscess
Периодический (5–29%)2
HP:0006485Agenesis of incisor
HP:0040019Finger clinodactyly

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