ANKS1Bは,子供の短身や成長障害を誘発する潜在的候補遺伝子です
Pankaj Prasun1, Rebecca C Pulvermacher1
1Department of Pediatrics, Division of Genetics, American Family Children's Hospital Madison, Madison, USA.
Journal of pediatric endocrinology & metabolism : JPEM
|August 26, 2025
まとめ
ANKS1B遺伝子の遺伝的欠損は,子供の短身や成長障害を引き起こす可能性があります. この発見は,小児の成長障害の既知の遺伝的原因を拡大します.
科学分野:
- 遺伝学
- 小児科
- 内分泌学
背景:
- 低身長と成長障害は,様々な病因を持つ小児の紹介の理由です.
- 遺伝的症候群は子供の身長が低い患者の約5%を占める.
- ゲノム技術により 成長障害に関連する遺伝子の識別が 増加しています
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