pseudohermaphroditism
101НЕДОСТАТОЧНОСТЬ ФЕРМЕНТОВ — мед. Синдромы врождённых нарушений обмена веществ встречаются редко, но оказывают значительное влияние на физическое, интеллектуальное, психическое развитие и качество жизни (например, фенилкетонурия, гомоцистинурия, гликогенозы, синдромы ломкой… …
102MPH — macroporous hydrogel; male pseudohermaphroditism; Master of Public Health; microtiter plate hybridization; milk protein hydrolysate * * * MPH abbr master of public health * * * Master of Public Health …
103gynandry — gyn·an·dry an drē n, pl dries HERMAPHRODITISM, INTERSEXUALITY specif the condition of the pseudohermaphroditic female in which the external genitalia simulate those of the male * * * gy·nan·dry (giґ ) (jĭґnan dre) 1. female… …
104intersex — in·ter·sex int ər .seks n an intersexual individual * * * n. an individual who shows anatomical characteristics of both sexes. See hermaphrodite, pseudohermaphroditism. • intersexuality n. * * * in·ter·sex (inґtər seks) 1. he …
105androgen insensitivity syndrome — a form of pseudohermaphroditism in which an individual who is genetically male (XY) has female external genitalia and secondary sexual characteristics but lacks female reproductive organs; testes are present internally. The syndrome is an X… …
106ambiguous genitalia — genital organs with characteristics typical of both male and female, as seen in hermaphroditism and some types of pseudohermaphroditism …
107gynandria — gy·nan·dria (gi ) (jə nanґdre ə) 1. female pseudohermaphroditism. 2. hermaphroditism. 3. masculinization in a female …
10811β-hydroxylase deficiency — 11β hy·drox·y·lase de·fi·cien·cy (hi drokґsə lās) an autosomal recessive disorder of steroidogenesis caused by a mutation in the CYP11B1 gene (locus: 8q21), which encodes steroid 11β monooxygenase; the resulting enzyme… …
10917α-hydroxylase deficiency — 17α hy·drox·y·lase de·fi·cien·cy (hi drokґsə lās) an autosomal recessive disorder of steroidogenesis caused by mutation in the CYP17A1 gene (locus: 10q24.3), which encodes steroid 17α monooxygenase; the resulting enzyme… …
11021-hydroxylase deficiency — 21 hy·drox·y·lase de·fi·cien·cy (hi drokґsə lās) an autosomal recessive disorder of steroidogenesis caused by mutation in the CYP21 gene (locus: 6p21.3) , which encodes steroid 21 monooxygenase, and the adjacent pseudogene CYP21P; the… …
