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  2. Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency

    en.wikipedia.org/wiki/Congenital_adrenal...

    The sex steroid deficiency produces effects similar to 17α-hydroxylase deficiency. Severely affected genetic females (XX) are born with normal internal and external genitalia and there are no clues to abnormality until adolescence, when the androgenic and estrogenic signs (e.g., breasts and pubic hair) of puberty either fails to occur or is ...

  3. ADAM17 - Wikipedia

    en.wikipedia.org/wiki/ADAM17

    ADAM17 is an 824-amino acid polypeptide.[5] [6]ADAM17 has multidomain structure that includes a pro-domain, a metallo-protease domain, a disintegrin domain, a cysteine-rich domain, an EGF-like domain, a transmembrane domain, and a cytoplasmic tail.

  4. Isolated 17,20-lyase deficiency - Wikipedia

    en.wikipedia.org/.../Isolated_17,20-lyase_deficiency

    The symptoms of isolated 17,20-lyase deficiency, in males, include pseudohermaphroditism (i.e., feminized, ambiguous, or mildly underdeveloped (e.g., micropenis, perineal hypospadias, and/or cryptorchidism (undescended testes)) external genitalia), female gender identity, and, in non-complete cases of deficiency where partial virilization occurs, gynecomastia up to Tanner stage V (due to low ...

  5. CYP17A1 - Wikipedia

    en.wikipedia.org/wiki/CYP17A1

    [22] [23] [24] Furthermore, mutations in the CYP17A1 gene are associated with rare forms of congenital adrenal hyperplasia, in particular 17α-hydroxylase deficiency/17,20-lyase deficiency and isolated 17,20-lyase deficiency. Overall, CYP17A1 is an important target for inhibition in the treatment of prostate cancer because it produces androgen ...

  6. Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

    en.wikipedia.org/wiki/Congenital_adrenal...

    Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency is a form of congenital adrenal hyperplasia (CAH) which produces a higher than normal amount of androgen, [1] resulting from a defect in the gene encoding the enzyme steroid 11β-hydroxylase (11β-OH) which mediates the final step of cortisol synthesis in the adrenal. 11β-OH CAH results in hypertension due to excessive ...

  7. 17β-Hydroxysteroid dehydrogenase III deficiency - Wikipedia

    en.wikipedia.org/wiki/17β-Hydroxysteroid...

    17β-Hydroxysteroid dehydrogenase III deficiency is a rare autosomal recessive disorder of sexual development condition that is a cause of 46,XY disorder of sex development (46,XY DSD). The impaired testosterone biosynthesis by 17β-hydroxysteroid dehydrogenase III (17β-HSD III), [ 6 ] [ 7 ] presents as atypical genitalia in affected males.

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    www.aol.com/lifestyle/shop-the-best-deals-at...

    It's the Walmart secret sale section that is full of Flash Deals on great items and brands, like Samsung TVs, bestselling headphones and top-rated air fryers. Quick Overview Carote Nonstick Pots ...

  9. ADAM7 - Wikipedia

    en.wikipedia.org/wiki/ADAM7

    11500 Ensembl ENSG00000069206 ENSMUSG00000022056 UniProt Q9H2U9 O35227 RefSeq (mRNA) NM_003817 NM_007402 RefSeq (protein) NP_003808 NP_031428 Location (UCSC) Chr 8: 24.44 – 24.53 Mb Chr 14: 68.73 – 68.77 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Disintegrin and metalloproteinase domain-containing protein 7 is a protein that in humans is encoded by the ADAM7 gene. ADAM7 is ...