Results 121 to 130 of about 553 (169)

Familial isolated 17,20-lyase deficiency in three siblings caused by a CYP17A1 mutation. [PDF]

Endocrinol Diabetes Metab Case Rep
Haider M, Rehman B, Sagri MN, Uneeb S, Memon F, Humayun KN.   +5 more
europepmc   +1 more source

Fertility in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a review. [PDF]

Front Endocrinol (Lausanne)
Roszkowska Z, Bobrowicz M, Betlejewska J, Hubska J, Rak-Makowska B, Ambroziak U.   +5 more
europepmc   +1 more source

Female Genital Cosmetic Surgery in Saudi Arabia: A Systematic Review of Awareness, Attitudes, Satisfaction, and Clinical Outcomes. [PDF]

Aesthet Surg J Open Forum
Sawan D, Alghamdi D.
europepmc   +1 more source

Case Report: unmasking pseudo-homozygosity in <i>CYP21A2</i>: intergenerational gene conversion expansion and the necessity of multimodal genetic testing. [PDF]

Front Endocrinol (Lausanne)
Altintas Z, Karaca S, Coskun A.
europepmc   +1 more source

Multidisciplinary emergent control of traumatic neovaginal bleeding after foreign-body insertion in the early postoperative period after gender-affirming vaginoplasty. [PDF]

Int J Crit Illn Inj Sci
Kashikar TS, McClung CD, Radomski MA, Joshi AK, Evans DC.   +4 more
europepmc   +1 more source

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

Ann Pediatr Endocrinol Metab
Yoon H, Kim D, Kim JH, Yoo HW, Choi JH.
europepmc   +1 more source

Development and use of a custom-designed vaginal dilator for post-surgical management in a congenital adrenal hyperplasia patient. [PDF]

Front Med (Lausanne)
Castelo-Branco C, Camacho M, Farré R.
europepmc   +1 more source