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2,791 Possible Causes for hydroxylase

  • Endocrine Dysfunction

    We present a case of a myelolipoma in conjunction with congenital adrenal hyperplasia secondary to 21-hydroxylase deficiency.[]

  • Adrenal Insufficiency

    RATIONALE: Adrenal incidentaloma is sometimes complicated with 21-hydroxylase deficiency (21-OHD). Latent nonclassical 21-OHD in incidentaloma is difficult to diagnose.[] Of the synthesis problems, congenital adrenal hyperplasia is the most common (in various forms: 21-hydroxylase , 17α-hydroxylase , 11β-hydroxylase and 3β-hydroxysteroid dehydrogenase[] Since serum aldosterone was below the reference range, more importantly, assessments for both antiadrenal antibodies and anti-21-hydroxylase antibodies were positive, she[]

  • Perry Syndrome

    We differentiated iPSCs into tyrosine hydroxylase (TH)-positive neurons. Immunocytochemistry analyses of control and mutant were performed.[] However, NK-1R, tyrosine hydroxylase (TH) and tryptophan hydroxylase (TrOH) immunoreactive neurons were significantly reduced in the ventrolateral medulla compared to controls[] Ishikawa T, Imamura K, Kondo T, Koshiba Y, Takahashi R, Takahashi J, Watanabe A, Fujii N, Tsuboi Y, Inoue H: Cytoplasmic aggregates of dynactin in iPSC-derived tyrosine hydroxylase-positive[]

  • Endometrial Hyperplasia

    OBJECTIVE: To report for the first time a case of postmenopausal endometrial hyperplasia caused by nonclassic 21-hydroxylase deficiency (NC21OHD).[]

  • Infertility

    Abstract We treated two patients with male infertility due to 21-hydroxylase deficiency.[] […] infertility and two unsuccessful previous attempts of ovarian stimulation for in vitro fertilization (IVF), whose nonclassic congenital adrenal hyperplasia (NC-CAH) due to 21-hydroxylase[]

  • Brain Stem Infarction

    Abstract The distribution of tyrosine hydroxylase (TH) and substance P (SP) was examined in the brain-stem of 4 infants with respiratory abnormalities associated with remote[] Acta Neurochirurgia 1999, 141: 209-213) ( 10536732 ) ErA9ahin Y. 1999 25 Aberrant distribution of tyrosine hydroxylase and substance P in infants with brain-stem infarction[]

  • Menstruation

    Abstract A patient with 17 alpha-hydroxylase deficiency (17OHD) who continued to menstruate is reported.[]

  • Secondary Myelofibrosis

    Abstract Prolyl hydroxylase (PH) is an important enzyme in collagen synthesis.[]

  • Ovulation

    PATIENT(S): Five females with salt-wasting 21-hydroxylase deficiency, aged 15.5 to 22.9 years; one had amenorrhea, one had irregular bleeding, and three had regular bleeding[] OBJECTIVE: To describe the case of a Japanese woman with combined 17alpha-hydroxylase/17,20-lyase deficiency (congenital adrenal hyperplasia type V) and to discuss possible[] CONCLUSION(S): These longitudinal data support the hypothesis that menstrual cycling in females with 21-hydroxylase deficiency can be prevented or disturbed by elevated progesterone[]

  • Penicillin G

    METHODS: Collagen metabolism of cultured dermal fibroblasts was studied by Northern hybridisation for mRNA of collagen I, proline-4-hydroxylase, lysyl hydroxylase, matrix[]

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