Results 21 to 30 of about 8,371 (167)

Idiopathic Male Pseudohermaphroditism Is Associated With Prenatal Growth Retardation.

, 2015
About 50% of intersex cases are due to male pseudohermaphroditism, and of these cases, 50% are not clarified aetiologically. The association of idiopathic male pseudohermaphroditism and prenatal growth retardation has been recently reported.
de Andrade Machado Neto, Francisco, Moreno Morcillo, André, Guerra-Junior, Gil, Trevas Maciel-Guerra, Andrea   +3 more
core   +2 more sources

Chromosomal Study is Must for Prepubertal Girl with Inguinal Hernia: Opportunity to Diagnose Complete Androgen Insensitivity Syndrome [PDF]

Journal of Clinical and Diagnostic Research, 2015
The sufferers of complete androgen insensitivity syndrome (CAIS) are phenotypic females despite of having functional testes and normal male karyotype.
Sudipto Konar, Debdeep Dasgupta, Dipak Kumar Patra, Angshuman De, Barindranath Mallick   +4 more
doaj   +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

First report of pseudohermaphroditism in cephalopods [PDF]

, 2006
Several malformations have been reported for cephalopods, involving a variety of internal and external structures. However, so far there are no published records of pseudohermaphroditism for the class.
N. Ortiz, Ortiz, Nicolás, Re, Maria Edith, M.E. Ré   +3 more
core   +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

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

DISORDERS OF SEXUAL DEVELOPMENT: UNDERSTANDING THE BASICS [PDF]

Kanem Journal of Medical Sciences, 2016
The enthusiasms on 'intersex' have been with humanity since antique. Inadequacies in the management of the condition backwash in Psychosocial and medical morbidities with occasional mortality.
Abdulkadir A
doaj  

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

Male pseudohermaphroditism in a dog: case report [PDF]

, 2023
Genital development disorders or anomalies have been described in several species of domestic animals. Sexual differentiation in mammals occurs sequentially and chronologically with the following distinct events in embryonic and faetal development: the ...
Soares, Paola Teles, Ribeiro, Apolônio Gomes, Bertoldo, Joselma da Silva Cavalcanti, Nascimento, Júlio Cézar dos Santos, Vilela, Liana Mesquita, Teixeira, Maria Juliana Coelho Dias da Silva   +5 more
core  

An insight into the landscape of a rare tumor-persistent Mullerian duct syndrome with testicular seminoma

Indian Journal of Pathology and Microbiology
Persistent Mullerian duct syndrome (PMDS) is a rare form of internal male pseudohermaphroditism in phenotypically males with 46 XY karyotype. The syndrome is caused by insufficient amount of Mullerian-inhibiting substance (MIS) or due to insensitivity of
Nibedita Sahoo, Abhijna Reddy, Manoranjan Khuntia   +2 more
doaj   +1 more source