生手 发表于 2025-3-21 16:27:58
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3-Methycrotonyl-CoA Carboxylase Deficiency: Types I and II,et al. 2001). Being a biotin-dependent enzyme, it can also be affected by inborn errors of biotin metabolism, such as multiple carboxylase or biotinidase deficiencies (Zempleni et al. 2019). Isolated 3-MCCD is subtyped as type I (OMIM #210200) and type II (OMIM #210210) based on the deficient subuni暂停,间歇 发表于 2025-3-22 06:31:29
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http://reply.papertrans.cn/39/3827/382632/382632_5.pngMundane 发表于 2025-3-22 13:56:05
,46, XY Sex Reversal (SRXY): Types 1–11,fected individuals are phenotypically normal females with XY karyotypes at birth. They have well-developed Mullerian structures and bilateral streak gonads instead of functional ovaries or testes; therefore, they do not develop secondary sexual characteristics and do not menstruate. People with SwyeMundane 发表于 2025-3-22 18:57:30
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http://reply.papertrans.cn/39/3827/382632/382632_8.pngMedicare 发表于 2025-3-23 04:42:46
Acephalic Spermatozoa Syndrome,ressive motility (Perotti and Gioria 1981). Most tails had normal structures with proximal centriole at anterior end covered by continuous plasma membrane (Perotti et al. 1981). Acephalic spermatozoa syndrome is a rare but severe type of monomorphic teratozoospermia (which is defined as the presence踉跄 发表于 2025-3-23 05:51:41
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