Results 31 to 40 of about 62 (53)

Ectopic Thyroid Tissue: A Case Series

open access: yesPhilippine Journal of Otolaryngology Head and Neck Surgery, 2013
Objective: To describe the clinical presentation and course of seven ectopic thyroid patients. Methods: Design: Retrospective Chart Review Setting: Tertiary Government Teaching Hospital Subjects: Seven patients Results: Five patients were ...
Somnath Saha   +3 more
doaj   +1 more source

Retrospective analysis of children with 46,XX testicular/ovotesticular DSD: a 10-year single-center experience

open access: yesFrontiers in Endocrinology
Purpose46,XX testicular/ovotesticular differences/disorders of sexual development (TDSD/OTDSD) are rare in childhood and exhibit marked distinctions compared to those in adulthood.
Yan Gong   +10 more
doaj   +1 more source

Gonadal Hormones and Retinal Disorders: A Review

open access: yesFrontiers in Endocrinology, 2018
AimGonadal hormones are essential for reproductive function, but can act on neural and other organ systems, and are probably the cause of the large majority of known sex differences in function and disease.
Raffaele Nuzzi   +4 more
doaj   +1 more source

A Gigantic Uterine Leiomyoma and Big Bilateral Adrenal Myelolipomas as a Result of Untreated Congenital Adrenal Hyperplasia

open access: yesAACE Clinical Case Reports, 2021
Introduction: Patients with congenital adrenal hyperplasia (CAH) can present early with salt wasting, adrenal insufficiency, and hyperandrogenism. Late consequences as a result of untreated CAH are now rarely seen.
Betty La, MD   +3 more
doaj  

Phenotypic spectrum and long-term outcomes of patients with 46,XX disorders of sex development [PDF]

open access: yesAnnals of Pediatric Endocrinology & Metabolism
Purpose 46,XX disorders of sex development (DSD) involve atypical genitalia accompanied by a normal female karyotype. This study was performed to investigate the clinical characteristics and long-term outcomes of patients with 46,XX DSD.
Heeyon Yoon   +4 more
doaj   +1 more source

Demystifying “steroid withdrawal” during remission in Cushing's disease: Is mineralocorticoid replacement the answer?

open access: yesIndian Journal of Endocrinology and Metabolism, 2019
Objective: To study renin-angiotensin-aldosterone axis status (RAAS) in patients of Cushing's disease (CD) at baseline and 6 weeks after curative trans-sphenoidal surgery and evaluate the role of mineralocorticoid replacement in the resolution of ...
Nimisha Jain   +4 more
doaj   +1 more source

CLINICAL CASE ADRENOGENITAL SYNDROME

open access: yesUkrainian Scientific Medical Youth Journal, 2017
The article describes clinical case Adrenogenital syndrome in child study hormonal and physical state which facilitated the correct treatment and solving legal issues for further life through legal sex change.
V.M. Yerokhovych, M.I. Bobryk
doaj  

Leydig Cell Hypoplasia: A Unique Paradox in the Diagnosis of 46, XY Disorders of Sex Development

open access: yesAACE Clinical Case Reports, 2020
: Objective: Disorders of sex development (DSD) are defined as conditions in which chromosomal sex is inconsistent with phenotypic sex, or in which the phenotype is not classifiable as either male or female.
Sharmin Jahan, FCPS, MD   +4 more
doaj  

Sensory neuron LKB1 mediates ovarian and reproductive function

open access: yesScientific Reports
Treatments for reproductive disorders in women consist of hormone replacement therapy, which have negative side effects that impact health, spurring the need to understand new mechanisms to employ new therapeutic strategies.
Melissa E Lenert   +2 more
doaj   +1 more source

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