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Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndrome

ORPHA:166024DiseaseAutosomal recessiveInfancy, Neonatal

Ассоциированные гены (1)

KIF7
kinesin family member 7
Disease-causing germline mutation(s) in
OMIM: 611254

Фенотипы (22)

Очень частый (80–99%)15
HP:0000207Triangular mouth
HP:0000256Macrocephaly
HP:0000316Hypertelorism
HP:0000431Wide nasal bridge
HP:0000767Pectus excavatum
HP:0000924Abnormality of the skeletal system
HP:0001249Intellectual disability
HP:0002007Frontal bossing
HP:0002419Molar tooth sign on MRI
HP:0002654Multiple epiphyseal dysplasia
HP:0002663Delayed epiphyseal ossification
HP:0002857Genu valgum
HP:0003037Enlarged joints
HP:0030084Clinodactyly
HP:0031092Spindle-shaped finger
Частый (30–79%)4
HP:0001274Agenesis of corpus callosum
HP:0002079Hypoplasia of the corpus callosum
HP:0002829Arthralgia
HP:0004322Short stature
Периодический (5–29%)2
HP:0002059Cerebral atrophy
HP:0012725Cutaneous syndactyly
Очень редкий (1–4%)1
HP:0003468Abnormal vertebral morphology

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