All individuals with variants in gene NCSTN

4 entries on 1 page. Showing entries 1 - 4.
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00229536 - PubMed: Wang 2010 3-generation family, 4 affecteds ? - China Chinese, Han - - - - ACNINV1 - 1 4 LOVD
00229537 - PubMed: Wang 2010 4-generation family, 13 affecteds, 1 asymptomatic carrier ? - China Chinese, Han - - - - ACNINV1 - 1 14 LOVD
00229538 - PubMed: Wang 2010 4-generation family, 8 affecteds ? - China Chinese, Han - - - - ACNINV1 - 1 8 LOVD
00399532 Fam9Pat9 PubMed: Kury 2022 - M - - - - - - - NDD weight 50 (-1.17), height 142 (-3.69), OFC 53 (-1.41 ); growth failure; developmental/intellectual delay; 2y-walk; speech delay, delayed first words, simple conversation; no hypotonia; seizure, 14y- tegretol treatment; 14y-MRI brain "empty sella"; behavioural anomalies, sensitive, difficulty with changes, treated with Risperdal; no cardiac anomalies; no eye anomalies; no urogenital/kidney anomalies; hands bilateral 3,4 fingers syndactyly; feet repair left vertical talus, wide big toes; scattered nevi; no feeding difficulties; facial dysmorphism, patchy alopecia almost complete from age 3 years - black hair, no eyebrows. Weakness left mouth angle, "scrotal tongue" with midline indentation, high arched palate, protruding auricles; hearing loss- perforation of eardrums, 22y-wearing hearing aids; alopecia 2 1 Johan den Dunnen
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