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  2. Congenital adrenal hyperplasia - Wikipedia

    en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia

    Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders characterized by impaired cortisol synthesis. [ 1 ] [ 2 ] It results from the deficiency of one of the five enzymes required for the synthesis of cortisol in the adrenal cortex . [ 3 ]

  3. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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

    Carriers for the alleles of the nonclassical forms may have no symptoms, such form of CAH is sometimes called cryptic form. [2] [3] Congenital adrenal hyperplasia due to 21-hydroxylase deficiency in all its forms accounts for over 95% of diagnosed cases of all types of congenital adrenal hyperplasia. [4]

  4. Congenital adrenal hyperplasia due to 11β-hydroxylase ...

    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 ...

  5. Hereditary carrier - Wikipedia

    en.wikipedia.org/wiki/Hereditary_carrier

    A hereditary carrier (genetic carrier or just carrier), is a person or other organism that has inherited a recessive allele for a genetic trait or mutation but usually does not display that trait or show symptoms of the disease. Carriers are, however, able to pass the allele onto their offspring, who may then express the genetic trait.

  6. 21-Hydroxylase - Wikipedia

    en.wikipedia.org/wiki/21-Hydroxylase

    Genetic variants in the CYP21A2 gene cause a disturbance in the development of the enzyme, leading to congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. Gene conversion events involving the functional gene and the pseudogene account for many cases of steroid 21-hydroxylase deficiency. [64] CAH is an autosomal recessive ...

  7. No criminal charges after 4 newborn bodies found in a freezer

    www.aol.com/news/no-criminal-charges-4-newborn...

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  8. Late onset congenital adrenal hyperplasia - Wikipedia

    en.wikipedia.org/wiki/Late_onset_congenital...

    Late onset congenital adrenal hyperplasia (LOCAH), also known as nonclassic congenital adrenal hyperplasia (NCCAH or NCAH), is a milder form of congenital adrenal hyperplasia (CAH), [1] a group of autosomal recessive disorders characterized by impaired cortisol synthesis that leads to variable degrees of postnatal androgen excess.

  9. Mother arrested in cold case death of newborn found in ...

    www.aol.com/news/mother-arrested-cold-case-death...

    The newborn baby girl was found by a man rummaging for recyclables in a dumpster behind a business in the 5400 block of La Sierra Avenue in Riverside on Oct. 13, 1987, Riverside Police said.