Results 31 to 40 of about 9,214 (219)

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  

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

Laparoscopic approach for gonadectomy in pediatric patients with intersex disorders [PDF]

, 2016
The birth of a child with a disorder of sex development (DSD) prompts a long-term management strategy that involves a myriad of professionals working with the family.
Calvo, Andres, Caprio, Maria Grazia, ESCOLINO, MARIA, ESPOSITO, CIRO, Roberti, Agnese, SETTIMI, ALESSANDRO   +5 more
core   +1 more source

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

The importance of genetic testing in adolescent-onset steroid-resistant nephrotic syndrome - Case report [PDF]

, 2014
Approximately 10-20% of children and 40% of adults with idiopathic nephrotic syndrome are steroid resistant and progress to end-stage renal disease requiring dialysis or renal transplantation.
Benoit, Benoit, Büscher, Büscher, Chernin, Chernin, Eddy, Eddy, Ehrich, Ehrich, Hinkes, Hinkes, Hoyer, Hoyer, Kerti, Kerti, Lipska, Lipska, Loirat, Loirat, Mekahli, Mekahli, Mucha, Mucha, Philippe, Philippe, Rood IM, Rood IM, Ruf, Ruf, Ruf, Ruf, Santin, Santin, Weber, Weber   +35 more
core   +2 more sources

Germ cell tumour of an undescended testis diagnosed in a patient with bilateral cryptorchidism presenting both male and female primary sex characteristics

Вестник урологии
Introduction. Testicular germ cell tumor (GCT) is a rare pathology that accounts for about 1% of all malignant neoplasms in men, while cryptorchidism is one of the main risk factors.
S. B. Petrov, A. V. Arnautov, K. A. Nikulina, S. A. Reva, A. D. Tsaregorodtseva, Yu. A. Tikhonova   +5 more
doaj   +1 more source

Managing disorder of sexual development surgically: A single center experience

Indian Journal of Urology, 2012
Introduction: Ambiguous genitalia are a major cause of parental anxiety and create psychological and social problems to patient, if not managed properly. Here we present our experience in managing patients with ambiguous genitalia. Material and Methods:
Jatinder Kumar, Vikas Kumar, Vijaylakshmi Bhatia, Preeti Dabadghao, Samit Chaturvedi, Rakesh Kapoor, M S Ansari   +6 more
doaj   +1 more source

Is there a causal association between genotoxicity and the imposex effect? [PDF]

, 2006
There is a growing body of evidence that indicates common environmental pollutants are capable of disrupting reproductive and developmental processes by interfering with the actions of endogenous hormones.
Josephine A. Hagger, Michael H. Depledge, Jörg Oehlmann, Susan Jobling, Tamara S. Galloway, Colborn T, Collins MKL, Cooke H, Depledge MH, Gibbs PE, Harring KE, Harris JO, Laruelle F, Smith BS   +13 more
core   +1 more source

Three novel mutations in the androgen receptor gene associated with partial androgen insensitivity syndrome: H570R, G589E and S759T [PDF]

Einstein (São Paulo), 2003
Three novel mutations in the androgen receptor gene were detectedby PCR-SSCP and characterized by DNA sequencing of genomicDNA samples from 3 unrelated patients with male pseudohermaphroditism caused by partial androgen insensitivity.
Patrícia Renovato Tobo, Angela Silva Barbosa, Lene Garcia Barbosa, Angela Maria Spínola-Castro, Carlos Alberto Moreira-Filho   +4 more
doaj  

Persistent Mullerian Duct Syndrome with Embryonal Cell Carcinoma along with Ectopic Cross Fused Kidney [PDF]

Journal of Clinical and Diagnostic Research, 2016
Persistent Mullerian Duct Syndrome (PMDS) is a form of internal male pseudohermaphroditism, where there is normal development of male secondary sexual characters, along with the presence of bilateral fallopian tubes and uterus.
ARUN KUMAR BARAD, NR MANJU BHARATH, V NARAYANA, V OM PRAMOD KUMAR RAJA, PRANAV REDDY JAMBULA   +4 more
doaj   +1 more source