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Goldberg–Shprintzen syndrome : ウィキペディア英語版 | Goldberg–Shprintzen syndrome
Goldberg–Shprintzen is a condition associated with mutations in ''KIAA1279'' gene which encodes KIF-binding protein (KBP), a protein that may interact with microtubules and actin filament. KBP may play a key role in cytoskeleton formation and neurite growth.〔http://hmg.oxfordjournals.org/content/22/12/2387.long#sec-9〕 Hirschsprung's disease may be part of the presentation. Individuals with the syndrome exhibit ocular (ptosis, hyperopia, or megalocornea), cardiac, urogenital (vesicoureteral reflux, multicystic renal dysplasia), and skeletal (oligodontia, scoliosis, high-arched palate) developmental abnormalities. ==References==
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