32 下列遺傳疾病與其特異性徵候之相關組合,何者最不可能?
(A)Miller-Dieker syndrome –lissencephaly/infantile seizure
(B)Angelman syndrome – rocker-bottom feet/clenched hand
(C)Waardenburg syndrome –heterochromia irides/piebaldism
(D)Prader-Willi syndrome – severe neonatal hypotonia/hypogonadism
(A)Miller-Dieker syndrome –lissencephaly/infantile seizure
(B)Angelman syndrome – rocker-bottom feet/clenched hand
(C)Waardenburg syndrome –heterochromia irides/piebaldism
(D)Prader-Willi syndrome – severe neonatal hypotonia/hypogonadism
答案:登入後查看
統計: A(9), B(40), C(14), D(8), E(0) #1054967
統計: A(9), B(40), C(14), D(8), E(0) #1054967
詳解 (共 5 筆)
#4070149
32 下列遺傳疾病與其特異性徵候之相關組合,何者最不可能?
(A)Miller-Dieker syndrome –lissencephaly/infantile seizure
(B)Angelman syndrome – rocker-bottom feet/clenched hand
(C)Waardenburg syndrome –heterochromia irides/piebaldism
(D)Prader-Willi syndrome – severe neonatal hypotonia/hypogonadism
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#6277322
(B)Angelman syndrome=>seizure , uncontrollable laughter, jerky movement
Trisomy18(Edwards syndrome)– rocker-bottom feet/clenched hand
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0
#6279397
Waardenburg syndrome
heterochromia irides虹膜異色症
Piebald Syndrome斑狀白化病
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0