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Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylation

ORPHA:254534Etiological subtypeAutosomal dominant, Not applicableInfancy, Neonatal

Ассоциированные гены (3)

DLK1
delta like non-canonical Notch ligand 1
Role in the phenotype of
OMIM: 176290
MEG3
maternally expressed 3
Role in the phenotype of
OMIM: 605636
RTL1
retrotransposon Gag like 1
Role in the phenotype of
OMIM: 611896

Фенотипы (19)

Очень частый (80–99%)7
HP:0001256Intellectual disability, mild
HP:0001263Global developmental delay
HP:0001561Polyhydramnios
HP:0005257Thoracic hypoplasia
HP:0006267Large placenta
HP:0006665Coat hanger sign of ribs
HP:0008872Feeding difficulties in infancy
Частый (30–79%)5
HP:0001252Hypotonia
HP:0001520Large for gestational age
HP:0001540Diastasis recti
HP:0002033Poor suck
HP:0008897Postnatal growth retardation
Периодический (5–29%)7
HP:0001518Small for gestational age
HP:0001537Umbilical hernia
HP:0001539Omphalocele
HP:0001548Overgrowth
HP:0001627Abnormal heart morphology
HP:0001629Ventricular septal defect
HP:0002194Delayed gross motor development

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