Image 1_Prenatal diagnosis of Prader–Willi syndrome via maternal UPD15 with placental mosaicism: incidental discovery of fetal DMD carrier status.jpeg

Image 1_Prenatal diagnosis of Prader–Willi syndrome via maternal UPD15 with placental mosaicism: incidental discovery of fetal DMD carrier status.jpeg

Background<p>Prader–Willi syndrome (PWS) represents a paradigm of genomic imprinting disorders. Given the severe lifelong complications of PWS, prenatal diagnosis is crucial for early intervention and genetic counseling.</p>Methods<p>Noninvasive prenatal testing (NIPT) indicated a...

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Bibliografske podrobnosti
Glavni avtor: Yanchou Ye (22523684) (author)
Drugi avtorji: Yiman Fu (22523687) (author), Zhechao Zhang (10290301) (author), Haofeng Ning (18361485) (author), Fangchao Tao (19922781) (author), Xiaonan Wang (276308) (author), Qun Fang (176267) (author), Zheng Chen (49483) (author), Xiulan Hao (12678556) (author)
Izdano: 2025
Teme:
Genetics
T15
UPD15
Prader–Willi syndrome
prenatal diagnosis
confined placental mosaicism
Duchenne muscular dystrophy
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