All individuals with variants in gene KIAA1244

2 entries on 1 page. Showing entries 1 - 2.
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00412362 Fam6 PubMed: Halvardson 2016 - F - Sweden - - - - - NDD psychomotor developmental dealy, generalized epilepsy, delayed speech development, encephalopathy 1 1 Johan den Dunnen
00428069 Pat8 PubMed: Paul 2023, Journal: Paul 2023 2-generation family, 1 affected, unaffected non carrier parents M - Israel Arab - - - - NDD brith at term, weight 3kg (50th%ile), , OFC 34 cm (50th%ile); absent speech; delayed gross motor development; severe delayed fine motor milestones; severe intellectual disability; seizures; autism; mild hypotonia; MRI brain subtle interdigitation of inferomedial frontal gyri; no behavior abnormalities; no failure to thrive; no feeding problems; no dysmotility; no hypoventilation; no vision/eye abnormalities; no hearing impairment; long palpebral fissures, small hands and feet; no congenital anomalies; ataxia 1 1 Johan den Dunnen
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