在一个家族中具有遗传KAT6A框架转移变异的表型变异性
Sidsel Bjerg Ringsted1, Sara Markholt1, Lotte Andreasen1
1Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.
European journal of medical genetics
|December 31, 2024
概括
KAT6A综合征是一种神经发育障碍,即使在家庭内,症状也会变化. 这项研究突出了一个具有遗传KAT6A变异的家族,揭示了更广泛的临床表现,包括正常的认知发育.
科学领域:
- 遗传学和分子生物学
- 神经发育障碍 神经发育障碍
- 临床遗传学 临床遗传学
背景情况:
- KAT6A综合征 (阿博莱达-坦综合征) 是一种神经发育障碍,其特点是智力障碍,发育迟缓,低血压和自闭症谱系障碍.
- 虽然通常与智力障碍有关,但最近的报道表明,在一些患有KAT6A综合征的个体中,正常的认知发展是可能的.
- 这种综合症是由KAT6A基因中的异合致病原体变异引起的,遗传变异很少见.
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