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Congenital adrenal hyperplasia (CAH) consists of a group of
disorders of adrenal steroidogenesis. Each disorder results from an
inherited deficiency of one of the several enzymes necessary for
normal steroid synthesis. The different enzyme deficiencies produce
characteristic patterns of hormonal abnormalities; the clinical
symptoms of the different forms of CAH depend on the particular
hormones that are deficient or that are produced in excess. The
earliest documented description of CAH was by DeCrecchio in 1865
(DeCrecchio 1865). This Neapolitan anatomist described a cadaver
having a penis with first degree hypospadias but no externally
palpable gonads. Dis- section revealed a vagina, uterus, fallopian
tubes, ovaries, and markedly enlarged adrenals. It is interesting
that the subject suffered a confusion of sex assignment, being
declared a female at birth and a male 4 years later. He conducted
himself as a male sexually and socially. Since the original
descrip- tion of this case, investigators have unravelled the
pathophysiology of the inborn errors of steroidogenesis. 1
Steroidogenesis and Enzymatic Conversions of Adrenal Steroid
Hormones A. Steroidogenesis The adrenal synthesizes three main
classes of hormones: mineralocorticoids (17-deoxy pathway),
glucocorticoids (17-hydroxy pathway), and sex steroids.
This is a reproduction of a book published before 1923. This book
may have occasional imperfections such as missing or blurred pages,
poor pictures, errant marks, etc. that were either part of the
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++++ The below data was compiled from various identification fields
in the bibliographic record of this title. This data is provided as
an additional tool in helping to ensure edition identification:
++++ Annual Report Of The Managers Of The Middletown State
Homeopathic Hospital: At Middletown, N.Y. To The State Commission
In Lunacy New York. State Homeopathic Hospital, Middletown
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