CONGENITAL ADRENAL HYPERPLASIAS
\kənd͡ʒˈɛnɪtə͡l ɐdɹˈiːnə͡l hˌa͡ɪpəplˈe͡ɪzi͡əz], \kəndʒˈɛnɪtəl ɐdɹˈiːnəl hˌaɪpəplˈeɪziəz], \k_ə_n_dʒ_ˈɛ_n_ɪ_t_əl ɐ_d_ɹ_ˈiː_n_əl h_ˌaɪ_p_ə_p_l_ˈeɪ_z_iə_z]\
Sort: Oldest first
-
A group of syndromes caused by inherited defects in cortisol (HYDROCORTISONE) and, in some types, ALDOSTERONE biosynthesis. Each of the several types that occur, such as simple virilizing forms (adrenogenital syndrome), salt-wasting forms, and virilizing hypertension forms may be caused by a variety of defects. Defects in 21-hydroxylase (STEROID 21-MONOOXYGENASE) are most common. Other defects occur in the enzymes 11 beta-hydroxylase (STEROID 11 BETA-MONOOXYGENASE), 17 alpha-hydroxylase (STEROID 17 ALPHA-MONOOXYGENASE), or 3-beta-hydroxysteroid dehydrogenase (3-HYDROXYSTEROID DEHYDROGENASES).
By DataStellar Co., Ltd
Word of the day
Quinones
- Hydrocarbon rings which contain two moieties position. They can be substituted in any position except at the ketone groups.
Nearby Words
- congenital abnormalities
- congenital abnormality
- congenital absence of brain
- congenital absence of cerebral hemispheres
- congenital adrenal hyperplasia
- Congenital Adrenal Hyperplasias
- congenital afibrinogenemia
- congenital amaurosis
- congenital amino acidopathies
- congenital amino acidopathy
- congenital amputation