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gnb5 in Homo sapiens | Mus musculus | Rattus norvegicus | All 482 Gene records
See gnb5 in MedGen (2)
Gnb5-related intellectual disability-cardiac arrhythmia syndrome
GNB5-related neurodevelopmental disorder (GNB5-NDD) is characterized by a spectrum of neurodevelopmental phenotypes that range from severe-to-profound intellectual disability (ID; 31/41 reported individuals), to mild-to-moderate ID (5/41), to normal intellect with severe language disorder (5/41, one extended family). A unique and specific feature of GNB5-NDD – regardless of neurodevelopmental phenotype – is nearly universal bradycardia caused by sinoatrial node dysfunction (sick sinus syndrome). Most individuals with severe and profound ID have a developmental and epileptic encephalopathy with focal seizures or epileptic spasms, as well as visual impairment (central or retinal) with nystagmus, difficulty feeding, and gastroesophageal reflux disease. The risk of early mortality is increased. [from GeneReviews]
Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia
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