All individuals with variants in gene CUL1

4 entries on 1 page. Showing entries 1 - 4.
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00081832 - - - F no Japan Japanese - - - - - - 1 1 Eri Imagawa
00296454 Fam1PatII1 PubMed: Imagawa 2017 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Japan - - - - - ? see paper; ... 1 1 Johan den Dunnen
00435602 Pat8 PubMed: Niggl 2023 2-generation family, 1 affected, unaffected non-carrier parents M - - - - - - - NDD see paper; ..., severe intra-uterine growth retardation, small placenta, thin cord, birth 36+6w; no speech; not walking; non-verbal; moderate-severe intellectual disability; delayed gross motor skills; delayed fine motor skills; absence seizures, generalized convulsions; hypotonia; no movement disorder; MRI multiple dysmorphisms cerebrum and cerebellum, delayed myelination (now normal), periventricul cysts, hypoplastic ICA; happy demeanor; obstructive sleep apnea; brachycephaly, head asymmetry, broad forehead, triangular face shape, broad nasal bridge, telecanthus, hypertelorism, downslanted palpebral fissures, bilateral ptosis, high palate, microretrognathia s/p distraction , dysmorphic ears , mottled appearance of skull with widened diplotic space (acquired) , undulate clavicles , pectus excavatum, 11 pairs of ribs; intermittent exotropia, mild myopia, low vision; moderate conductive hearing impairment, stenosis of external auditory canal; GER dysphagia, G-tube, constipation; no recurrent infections; atrial septal defect; PFO, aortic root dilatation, pyloric stenosis, paraesophageal hernia, bilateral cryptorchidism, micropenis; laryngomalacia; tracheobronchomalacia; asthma; growth hormone deficiency 1 1 Johan den Dunnen
00438627 HSC0104 PubMed: Hamdan 2017 WGS analysis 197 individuals with unexplained DEE (unaffected parents) - - Canada - - - - pharmaco-resistant seizures DEE - 1 1 Johan den Dunnen
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