Identification of a novel KISS1R (GPR54) gene variant (c.505+2T>G) in a patient with congenital hypogonadotropic hypogonadism: A case report and literature review. [PDF]
Exp Ther MedMenekse B +7 more
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From Severe Virilization to Precocious Puberty in a 46,XX Patient: Therapeutic Challenges in a Case of 11β-Hydroxylase Deficiency. [PDF]
CureusHamaichat M +3 more
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Fertility in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a review. [PDF]
Front Endocrinol (Lausanne)Roszkowska Z +5 more
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Bilateral Ovarian Steroid Cell Tumor With One-Year Disease-Free Follow-Up: A Case Report. [PDF]
CureusMuñoz L +4 more
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Gender-affirming care during lactation: Case report of a transmasculine parent. [PDF]
Can Fam PhysicianOladimeji D, Adams B, Eastman L.
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Diagnostic challenges of androgen secreting tumor by sclerosing stromal tumor: A case report. [PDF]
Int J Surg Case RepHarzif AK +5 more
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Apparent Clitoromegaly in a Newborn: A Case of Congenital Adrenal Hyperplasia. [PDF]
CureusSvanadze M +4 more
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Comprehensive characterization of 21-hydroxylase deficiency in a Chinese pediatric cohort: phenotype, steroid profiles and genetics. [PDF]
Front Endocrinol (Lausanne)Chong H +7 more
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Prostatic development and verumontanum in a 46,XX karyotype : An embryological paradox redefining diagnostic algorithm for testicular DSD. [PDF]
Urol Case RepMuhammad RY, Pitoyo J.
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