All individuals with variants in gene DACH2

6 entries on 1 page. Showing entries 1 - 6.
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00000208 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), no prolactin deficiency, age sonographic determination testicular volume 17.64y, testicular volume right/left 21/20 (7.3–16ml) 14 1 Yu Sun
00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 15 1 Yu Sun
00045137 - - hemizygote patient, mother heterozygous carrier M no Estonia white - - yes - ID, MRX;IDX ID, epilepsy, scoliosis, spasticity (hypotonia in infancy), hyperkinetic movements; severe intellectual disability (HP:0010864); global developmental delay (HP:0001263); motor delay (HP:0001270) 1 1 Sander Pajusalu
00173572 19377476-Pat? PubMed: Tarpey 2009 - M - - - - - for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX;IDX - 1 1 Lucy Raymond
00173596 19377476-Pat? PubMed: Tarpey 2009 - M - - - - - for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX;IDX - 1 1 Lucy Raymond
00226142 FamPatIII1 PubMed: Shukla 2019, Journal: Shukla 2019 3-generation family, unaffected heterozygous carrier parents M - India - - - - - RPIAD see paper; ..., developmental delay; speech delay; epilepsy; regression; dysarthria; no nystagmus; ataxia; spasticity; exaggerated deep tendon reflexes; extensor plantar reflex; increased urine polyol levels; retinitis pigmentosa; cerebral white matter abnormalities; no hearing loss; EEG slow right frontal discharge with epileptiform activity 1 1 Anju Shukla
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