scholarly journals INTERSEX STATE WITH TESTICULAR FEMINIZATION SYNDROME: A CASE REPORT AND REVIEW OF LITERATURE.

2020 ◽  
pp. 1-2
Author(s):  
Parul Garg ◽  
Ishwer Tayal
Keyword(s):  
Sexual Behavior ◽  
Case Report ◽  
Rare Disease ◽  
X Chromosome ◽  
Reproductive Organs ◽  
Androgen Insensitivity Syndrome ◽  
Testicular Feminization ◽  
Review Of Literature ◽  
Androgen Insensitivity ◽  
Physical Form

Intersex state is a state in which intermingling of characters of both sexes present to varying degrees, including physical form, reproductive organs and sexual behavior. Testicular feminization, or the androgen insensitivity syndrome, is a rare disease. Because of various abnormalities of the X chromosome, a male, genetically XY, has some physical characteristics of a woman or a full female phenotype.

scholarly journals A Case Report Based On Complete Androgen Insensitivity Syndrome

2020 ◽  
Author(s):  
pengju li ◽  
jiefei xiao ◽  
junhang luo ◽  
wei chen
Keyword(s):  
Case Report ◽  
Medical History ◽  
Rare Disease ◽  
Multidisciplinary Approach ◽  
Androgen Insensitivity Syndrome ◽  
Surgical Removal ◽  
Case Presentation ◽  
Complete Androgen Insensitivity Syndrome ◽  
Androgen Insensitivity ◽  
Appropriate Care

Abstract Background: Androgen insensitivity syndrome (AIS) is a rare disease caused by mutations in the AR gene. This results in resistance to the actions of androgen as well as a female phenotype with 46 XY. Anatomically, individuals with AIS lack both a uterus and ovaries. Case presentation: In this case report, we detail a 32-year-old patient with complete AIS (CAIS). This female patient with 46 XY genotype came to our hospital seeking surgical removal of bilateral testis. The subsequent medical history, clinical examination, imaging, and endocrine outcomes from this patient were collected and are presented here. Conclusions: Individuals with CAIS need appropriate care from doctors and support from their family. The diagnosis, treatment, and management of CAIS also requires a multidisciplinary approach.

New mutation causing androgen insensitivity syndrome – a case report and review of literature

2018 ◽  
Vol 35 (4) ◽  
pp. 294-297 ◽  
Author(s):  
Marzena Maciejewska-Jeske ◽  
Patrycja Rojewska-Madziala ◽  
Karolina Broda ◽  
Karolina Drabek ◽  
Anna Szeliga ◽  
...  
Keyword(s):  
Case Report ◽  
Androgen Insensitivity Syndrome ◽  
Review Of Literature ◽  
New Mutation ◽  
Androgen Insensitivity

scholarly journals An Uncommon Presentation of Myasthenia Gravis with Thymoma - A Case Report and Review of Literature

1970 ◽  
Vol 13 (1) ◽  
pp. 109-114
Author(s):  
MA Hannan ◽  
Mohammad Sayeed Hassan ◽  
Ayesha Begum ◽  
AKM Nurul Kabir
Keyword(s):  
Case Report ◽  
Neuromuscular Junction ◽  
Myasthenia Gravis ◽  
Diurnal Variation ◽  
Rare Disease ◽  
Liquid Food ◽  
Review Of Literature ◽  
Upper Arm ◽  
Uncommon Presentation ◽  
Incorrect Diagnosis

Myasthenia Gravis (MG) is a rare disease of neuromuscular junction which typically presents with fatigable weakness of cranial and limb muscles. But patient may present with vague symptoms which may mislead physicians to an incorrect diagnosis. We are reporting a 45 year old cobbler presented with the complaints of lack of energy, aching pain in shoulder, back, upper arm and difficulty in swallowing of both solid and liquid food without any diurnal variation for two and half years. He was ultimately diagnosed as a case of MG and thymectomy revealed thymoma. DOI: http://dx.doi.org/10.3329/jom.v13i1.10087 JOM 2012; 13(1): 109-114

Androgen Insensitivity Syndrome: Case Report With Review of the Literature

2011 ◽  
Vol 04 (03) ◽  
Author(s):  
Gajanan Bhat ◽  
Muralidhar Belur Raviraj ◽  
Srinivas Jayaram ◽  
Indukala Siddalingaiah
Keyword(s):  
Case Report ◽  
Androgen Insensitivity Syndrome ◽  
Review Of The Literature ◽  
Androgen Insensitivity
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