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Grubben-de Cock-Borghgraef syndrome

ORPHA:2101Malformation syndromeAntenatal, Neonatal

Фенотипы (15)

Очень частый (80–99%)15
HP:0000164Abnormality of the dentition
HP:0000311Round face
HP:0000470Short neck
HP:0000496Abnormality of eye movement
HP:0000592Blue sclerae
HP:0000750Delayed speech and language development
HP:0000958Dry skin
HP:0000964Eczematoid dermatitis
HP:0001250Seizure
HP:0001252Hypotonia
HP:0001263Global developmental delay
HP:0001315Reduced tendon reflexes
HP:0001338Partial agenesis of the corpus callosum
HP:0004097Deviation of finger
HP:0200055Small hand

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