<nowiki>Síndrome de Pallister-Killian; パリスター・キリアン症候群; syndrome de Pallister-Killian; Zespół Pallistera-Killiana; Pallister–Killian syndrome; Sindrome di Pallister-Killian; Pallister-Killian-Syndrom; Pallister-Killianin oireyhtymä; Pallister–Killian syndrome; متلازمة باليستر-كيليان; Pallister-Killian sendromu; Pallister-Killianov sindrom; sindrome genetica; maladie; rare disease; اضطراب وراثي نادر; genetycznie uwarunkowany zespół wad wrodzonych; seltene Krankheit; Sindrome di Pallister Killian; Teschler-Nicola-Syndrom; Pallister-Mosaik-Syndrom; Tetrasomie 12p Mosaik; Pallister-Killianin syndrooma; Isochromosome 12p syndrome; Pallister-Killian syndrome; Hexasomy 12P, Mosaic; Tetrasomy type 12p; PALLISTER-KILLIAN SYNDROME; PKS; Tetrasomy 12P, Mosaic; Isochromosome 12p mosaicism; PKS; فسيفسائية التصبغ الرباعي 12p; متلازمة باليستر لاختلال الصيغة الصبغية الفسيفسائي; Sindrome de Pallister Killian; Síndrome de Pallister Killian; Sindrome de Pallister-Killian; tétrasomie 12p</nowiki>
Pallister–Killian syndrome rare disease |
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| Instance of | - rare disease
- developmental defect during embryogenesis
- class of disease
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| 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
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| Named after | - Philip David Pallister
- Maria Teschler-Nicola
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Pallister Killian Syndrome clinical features of PKS.png 512 × 448; 481 KB