Cargando…

Mosaic triple X syndrome in a female with primary amenorrhea

BACKGROUND: Turner's syndrome is the most common chromosomal abnormality in females, affecting 1 in 2,500 live female births. It is a result of absence of an X chromosome or the presence of a structurally abnormal X chromosome. Its most consistent clinical features are short stature and ovarian...

Descripción completa

Detalles Bibliográficos
Autores principales:	Venkateshwari, A., Srimanjari, K., Srilekha, A., Begum, Ashrafunnisa, Sujatha, M., Sunitha, T., Nallari, Pratibha, Jyothy, A.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2012
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3491304/ https://www.ncbi.nlm.nih.gov/pubmed/23162306 http://dx.doi.org/10.4103/0971-6866.100790

Ejemplares similares

A Rare De Novo Balanced X; 1 Translocation in an Indian Female with Primary Amenorrhea
por: Venkateshwari, Ananthapur, et al.
Publicado: (2015)

A Robertsonian Translocation rob (14;15) (q10:q10) in a Patient with Recurrent Abortions: A Case Report
por: Venkateshwari, Ananthapur, et al.
Publicado: (2010)

A Dysmorphic Child with a Pericentric Inversion of Chromosome 8
por: Ananthapur, Venkateshwari, et al.
Publicado: (2012)

Association of CYPA1 gene polymorphism with plasma nitric oxide levels in COPD
por: Begum, Ashrafunnisa, et al.
Publicado: (2014)

Role of Proteases and Antiprotease in the Etiology of Chronic Pancreatitis
por: Kavutharapu, Srimanjari, et al.
Publicado: (2012)

A Novel Familial Case Report of Genetic Syndrome Mimicking Congenital TORCH infections; Pseudo-TORCH Syndrome 2
por: Sehrish, Iram, et al.
Publicado: (2022)

Evaluation of Interleukin-10 (G-1082A) Promoter Polymorphism in Preeclampsia
por: Sowmya, Sabnavis, et al.
Publicado: (2013)

Transferrin (rs3811647) gene polymorphism in iron deficiency anemia
por: Manjari, K Sri, et al.
Publicado: (2014)

Epidermolysis Bullosa: A Report of Three Cases with Novel Heterozygous Deletions in PLEC and Homozygous Non sense Mutations in COL7A1 Genes
por: Tella, Sunitha, et al.
Publicado: (2022)

Association of matrix metalloproteinase -7 (-181A/G) promoter polymorphism in chronic pancreatitis
por: Manjari, K. Sri, et al.
Publicado: (2014)

A Common SNP of IL-10 (-1082A/G) is Associated With Increased Risk of Premenopausal Breast Cancer in South Indian Women
por: Vinod, Cingeetham, et al.
Publicado: (2015)

BRIP1/FANCJ Mutation Analysis in a Family with History of Male and Female Breast Cancer in India
por: Venkateshwari, Ananthapur, et al.
Publicado: (2017)

Role of Interstitial Collagenase Gene Promoter Polymorphism in the Etiology of Gastric Cancer
por: Devulapalli, Krishnaveni, et al.
Publicado: (2014)

45, X/ 46, X, psu idic (Y) (q11.2) Mosaicism in a Primary Amenorrhea Girl with Swyer Syndrome
por: Han, Yu, et al.
Publicado: (2023)

Significant Association of Interleukin4 Intron 3 VNTR Polymorphism with Susceptibility to Gastric Cancer in a South Indian Population from Telangana
por: Bhayal, Amar Chand, et al.
Publicado: (2015)

Role of Tumor Necrosis Factor-α -308 G/A Promoter Polymorphism in Gastric Cancer
por: Bhayal, Amar C., et al.
Publicado: (2013)

45,X/46,XY Mosaicism in an 18-year-old Girl with Primary Amenorrhea : A Case Report*
por: Lau, Eunice Yi Chwen, et al.
Publicado: (2020)

A novel insertion-induced frameshift mutation of the androgen receptor gene in a patient with primary amenorrhea()
por: Sharma, Vikas, et al.
Publicado: (2013)

Impact of Genetic Variants in Estrogen Receptor-β Gene in the Etiology of Uterine Leiomyomas
por: Bharathi, Chitroju, et al.
Publicado: (2019)

A 19-year-old Female with Primary Amenorrhea
por: Khanna, Tanvi, et al.
Publicado: (2021)

Clinical profile and cytogenetic correlations in females with primary amenorrhea
por: Chandel, Divya, et al.
Publicado: (2023)

The Mysteries of Primary Amenorrhea: Swyer Syndrome
por: Cherukuri, Srinidhi, et al.
Publicado: (2022)

Constrictive Pericarditis and Primary Amenorrhea with Syndactyly in an Iranian Female: Mulibrey Nanism Syndrome
por: Davarpasand, Tahereh, et al.
Publicado: (2016)

A Case of Primary Amenorrhea with Swyer Syndrome
por: Priya, Pritti K., et al.
Publicado: (2017)

Association of Interleukin-10 Promoter Polymorphism (-1082 G/A) and Gastric Cancer in Andhra Pradesh Population of South India
por: Chand-Bhayal, Amar, et al.
Publicado: (2012)

The Genetic Bases of Uterine Fibroids; A Review
por: Medikare, Veronica, et al.
Publicado: (2011)

miRNA regulation during cardiac development and remodeling in cardiomyopathy
por: Chaitra, K.L., et al.
Publicado: (2013)

Medically induced amenorrhea in female astronauts
por: Jain, Varsha, et al.
Publicado: (2016)

A 19-year-old Female with Primary Amenorrhea: Mayer–Rokitansky–Küster–Hauser Syndrome
por: Khanna, Tanvi, et al.
Publicado: (2021)

SUN-069 A 14 Year Old Female with Primary Amenorrhea
por: Chakravarthy, Varshini, et al.
Publicado: (2020)

Primary Amenorrhea With Hypothyroidism: Finding the Cause
por: Alvi, Asim Munir, et al.
Publicado: (2021)

An Unusual Cause of Primary Amenorrhea
por: Marenych, Nadiia, et al.
Publicado: (2021)

Mullerian Agenesis with Primary Amenorrhea: A Case Report of a Normal Phenotypic Female
por: Ajiboye, Akinyosoye D., et al.
Publicado: (2017)

Risperidone-Induced Amenorrhea in Floridly Psychotic Female
por: Shagufta, Shanila, et al.
Publicado: (2017)

Prevalence of amenorrhea in elite female competitive climbers
por: Joubert, Lanae, et al.
Publicado: (2022)

Amenorrhea
Publicado: (1854)

A rare cause for primary amenorrhea: Sporadic perrault syndrome
por: Ameen, K. H. Noorul, et al.
Publicado: (2012)

Genotype–phenotype correlation in long QT syndrome families
por: Qureshi, Sameera Fatima, et al.
Publicado: (2015)

Cytogenetic investigation of patients with primary amenorrhea
por: Laxmi, K. Vijaya, et al.
Publicado: (2012)

True hermaphrodite presenting as primary amenorrhea
por: Palo, Lal Bahadur, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_tks75houaqnhljeno8epe6j0iq