Results 21 to 30 of about 9,214 (219)

Dysgerminoma in Pseudohermaphroditism: A Case Report

Nepalese Medical Journal, 2020
Female pseudohermaphroditism occurs when normal ovaries are present but the body is partially masculinized as individuals with congenital adrenal hyperplasia, also known as adrenogenital syndrome. This is an inherited disorder that accounts for about one-
Rashmey Pun, Sujata Pudasaini, Rita Mahaseth, Kriti Shrestha   +3 more
doaj   +1 more source

Complexities of gender assignment in 17β-hydroxysteroid dehydrogenase type 3 deficiency: is there a role for early orchiectomy? [PDF]

, 2013
BACKGROUND: 17β-Hydroxysteroid dehydrogenase type-3 (17βHSD-3) deficiency is a rare cause of 46,XY disorders of sex development. The enzyme converts androstenedione to testosterone, necessary for masculinization of male genitalia in utero.
Amy Vallerie, Howard M Saal, Janet Chuang, Lesley Breech, Meilan M Rutter, Peggy Crawford, Shumyle Alam   +6 more
core   +1 more source

Persistent Mullerian duct syndrome (PMDS): Case report and review of literature

Urology Case Reports, 2022
Persistent Mullerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism (MPH) which characterized by the presence of uterus, fallopian tubes and upper part of vagina in an otherwise normally differentiated 46, XY male.
Abdullah B. Alanazi, Afrah Aldhowayan, Mousa M. Almuhanna, Abdullah M. Alghamdi   +3 more
doaj   +1 more source

Male pseudohermaphroditism in dogs: three case reports

Veterinární Medicína, 2007
Three Cocker Spaniel dogs, 2-3 months old, weighing 3-4 kg, were presented to the Chonbuk Animal Medical Centre, Chonbuk National University, with intersex anomalies.
M.R. Alam, Y.G. Cho, S.J. Cho, J.I. Lee, H.B. Lee, H.J. Tae, I.S. Kim, N.S. Kim   +7 more
doaj   +1 more source

Normal sex differences in prenatal growth and abnormal prenatal growth retardation associated with 46,XY disorders of sex development are absent in newborns with congenital adrenal hyperplasia due to 21-hydroxylase deficiency [PDF]

, 2011
Background Congenital adrenal hyperplasia due to 21-hydroxylase deficiency is the most common presentation of a disorder of sex development (DSD) in genetic females. A report of prenatal growth retardation in cases of 46,XY DSD, coupled with observations
Laura J Chalmers, Paul Doherty, Claude J Migeon, Kenneth C Copeland, Brianna C Bright, Amy B Wisniewski   +5 more
core   +2 more sources

Persistent Mullerian duct syndrome with testicular seminoma: A report of two cases

Indian Journal of Urology, 2011
Persistent Mullerian duct syndrome is a rare form of male pseudohermaphroditism, characterized by the presence of the Mullerian duct structures in an otherwise phenotypically as well as genotypically normal male.
Renuka V Inuganti, G Saila Bala, Y Kiran Kumar, Y Krishna Bharathi   +3 more
doaj   +1 more source

Persistant Mullerian duct syndrome with intra-abdominal seminoma

Urology Case Reports, 2020
Persistent Mullerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism; it is defined by the presence of the Mullerian duct derivatives (the uterus, the fallopian tubes, and the upper vagina) in genotypically and phenotypically males ...
Ali Al-Asmar, Adnan Abu-Qamar, Nizar Al-saidah, Awad Al-Kaabneh, Ayman Al-Qaralleh, Ahmad Al-Hiari   +5 more
doaj   +1 more source

Persistent mullerian duct syndrome in a patient with bilateral cryptorchid testes with seminoma

Journal of Human Reproductive Sciences, 2012
Persistent mullerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism in which mullerian duct derivatives are present in an otherwise normally differentiated 46 XY male.
Shrinivasan Chamrajan, Nidhi H Vala, Jatin R Desai, Niraj N Bhatt   +3 more
doaj   +1 more source

Renal Subcapsular xenografing of human fetal external genital tissue - A new model for investigating urethral development. [PDF]

, 2017
In this paper, we introduce our novel renal subcapsular xenograft model for the study of human penile urethral and clitoral development. We grafted fifteen intact fetal penes and clitorides 8-11 weeks fetal age under the renal capsules of gonadectomized ...
Baskin, Laurence, Cao, Mei, Cunha, Gerald, Isaacson, Dylan, Shen, Joel, Sinclair, Adriane, Yue, Xuan   +6 more
core   +2 more sources

46, XY Complete Gonadal Dysgenesis (Swyer Syndrome) Presenting as Primary Amenorrhea in a Normomorphic Adult Female From Kakamega, Kenya. [PDF]

Clin Case Rep
ABSTRACT Differences/disorders of sex development (DSDs) are a diverse group of congenital conditions that result in disagreement between an individual's sex chromosomes, gonads, and/or anatomical sex. The 46, XY DSD group is vast and includes various conditions caused by genetic variants, hormonal imbalances, or abnormal sensitivity to testicular ...
Omoaghe C.
europepmc   +2 more sources