All individuals with variants in gene CC2D1A

4 entries on 1 page. Showing entries 1 - 4.
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00000029 - PubMed: Almomani 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00292050 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 14 Mohammed Faruq
00292051 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 8 Mohammed Faruq
00408966 ? PubMed: Tuncel 2021 - M no - Turkish Cypriot - - - - JBTS delayed motor and cognitive milestones; neonatal episodic hyperpnea and hypotonia in early childhood; neurological examination: inability to initiate voluntary saccades in a head-fixed position, while saccades can be initiated by the vestibulo-ocular reflex, which is suggestive of oculomotor apraxia and truncal ataxia. Brain magnetic resonance imaging: cerebellar vermis hypoplasia, mesencephalon, and superior cerebellar peduncles - typical molar tooth sign; 15y psychiatric symptoms: repetitive questions, extreme anxiety and anger when not answered, worrying about getting sick; .evaluation: moderate intellectual disability and obsessive-compulsive disorder; retinal examination and abdominal ultrasonography: normal (retinal dystrophy, ocular coloboma, cystic renal disease, and hepatic fibrosis were excluded) 1 1 LOVD
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