Category:Pallister–Killian syndrome

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Pallister–Killian syndrome 
rare disease
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Instance of rare disease,
developmental defect during embryogenesis
Subclass of Tetrasomy,
syndromic diaphragmatic or thoracic malformation,
chromosomal anomaly with epilepsy as a major feature,
chromosomal disease with overgrowth,
syndromic diaphragmatic or abdominal wall malformation,
syndromic anorectal malformation,
partial trisomy/tetrasomy of the short arm of chromosome 12
Authority control
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Sindrome di Pallister-Killian (it); syndrome de Pallister-Killian (fr); Zespół Pallistera-Killiana (pl); Pallister–Killian syndrome (nl); Pallister-Killian-Syndrom (de); Pallister-Killianin oireyhtymä (fi); Pallister–Killian syndrome (en); متلازمة باليستر-كيليان (ar); Síndrome de Pallister-Killian (es) rare disease (en); genetycznie uwarunkowany zespół wad wrodzonych (pl); maladie (fr); اضطراب وراثي نادر (ar) Sindrome di Pallister Killian (it); Tetrasomie 12 p, Teschler-Nicola-Syndrom, Pallister-Mosaik-Syndrom (de); Pallister-Killianin syndrooma (fi); Isochromosome 12p syndrome, Pallister-Killian syndrome, Hexasomy 12P, Mosaic, Tetrasomy type 12p, PALLISTER-KILLIAN SYNDROME; PKS, Tetrasomy 12P, Mosaic, Isochromosome 12p mosaicism, PKS (en); متلازمة باليستر لاختلال الصيغة الصبغية الفسيفسائي), فسيفسائية التصبغ الرباعي 12p (ar); Sindrome de Pallister Killian, Síndrome de Pallister Killian, Sindrome de Pallister-Killian (es); tétrasomie 12p (fr)

Media in category "Pallister–Killian syndrome"

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