dysgenesis|dysgeneses in English

noun

abnormal development of an orga

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1. Conclusion MRI is the best method to diagnose the dysgenesis of the corpus callosum.

2. Objective To study the CT and MRI findings of Dysgenesis of the Corpus Callosum.

3. In this case, the androgen insensitivity syndrome or the adrenogenital syndrome, as well as gonadal dysgenesis (e.g.

4. British Columbia has high rates in three categories: cleft palate with cleft lip, renal agenesis and dysgenesis, and Down's syndrome.

5. Handlings are given to differentiate the “stippled epiphyses” from the achondroplasia, the dysplasia epiphysialis multiplex and the cretinoid epiphysial dysgenesis.

6. Methods The imaging findings of 9cases Dysgenesis of the Corpus Callosum diagnosed by computed tomography(CT)and magnetic resonance imaging(MRI)were analysed retrospectively.

7. Chromosome aberrations, XX and XY gonadal dysgenesis, mutations of the gonadotropin receptor genes, disorders of steroid hormone biosynthesis, agonadism, and autoimmune diseases have to be considered.

8. Total “ovarian” gonadal dysgenesis in individuals withmale nuclear sex is postulated as the cause of the hitherto so-calledgonadal agenesis (Turner's syndrome), as there is some evidence that the “gonadal streaks” in these cases represent rudimentary ovaries.

9. Cretin Congenital hypothyroidism Endocrinology A person with defective thyroxine or thyroglobulin synthesis Etiology Goiter, iodine deficiency in the mother while pregnant; thyroid gland defects–aplasia, hypoplasia or dysgenesis Clinical Cold intolerance, serosal effusions, myxedema, ↓ metabolic rate, ↑ cholesterol, profound mental retardation–hypothyroid idiocy, ↓ growth.

10. Anencephalus and similar anomalies Spina bifida Encephalocele Congenital hydrocephalus Transposition of great vessels Hypoplastic left heart syndrome Cleft palate Cleft palate with cleft lip Tracheo-esophageal fistula, esophageal atresia and stenosis Atresia and stenosis of large intestine, rectum and anal canal Renal agenesis and dysgenesis Reduction of limb Anomalies of abdominal wall Down’s syndrome

11. However, adequate androgen secretion alone does not ensure normal sexual hair development in many patients with gonadal dysgenesis. Moreover, in children with a lack or delayed adrenarche long-term treatment with DHAS at dosages such as to restore normal levels for age, failed to induce growth of sexual hair or any change in growth rate, bone maturation velocity, or to advance puberty.

12. Intersexuality is an umbrella term for a multitude of diagnoses having different causes, different disease patterns and different developments. Some of them are described in this article, such as the adrenogenital syndrome showing virilisation phenomena with a 46,XX chromosome set or reduced virilisation with a 46,XY chromosome set in the case of an androgen insensitivity syndrome, disturbances of androgenic biosynthesis or gonadal dysgenesis mostly with a feminine gender role.