All individuals with variants in gene TTI2

4 entries on 1 page. Showing entries 1 - 4.
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00001639 FamPatIII2/5/9 PubMed: Langouet 2013, Journal: Langouet 2013 3-generation family, 3 affected (2F, M), unaffected heterozygous carrier parents/relatives F;M yes Algeria - - - - - ID see paper; ..., born normal growth parameters, an unremarkable pregnancy/delivery, uncomplicated neonatal period; 30–36y, occipitofrontal circumference −3 to −4SD, severe cognitive impairment, severe speech delay, behavioral disturbances, no seizures, short stature, vertebral anomalies, sloping forehead, deep set eyes, anteverted large ears; normal circulating T, B, NK cell counts, mild naive T (CD4, CD8) lymphocytopenia; neurological examination normal, molecular karyotyping normal, normal metabolic workup; severe intellectual disability (HP:0010864); severe speech delay (HP:0000750) 1 3 Laurence Colleaux
00229561 FamM100 PubMed: Najmabadi 2011 family, 4 affected - yes Iran - - - - - ID non-syndromic intellectual disability; moderate intellectual disability (HP:0002342) 1 4 Johan den Dunnen
00294628 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00361508 14DG0038 PubMed: Anazi 2017 simplex case F yes Saudi Arabia - - - - - ID not syndromic; intellectual disability and boarderline microcephaly 1 1 Johan den Dunnen
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