Cargando…

Genetic Investigation of 261 Cases of Turner Syndrome Patients Referred to the Genetic Clinic

BACKGROUND: Turner syndrome (TS), also known as 45,X, is a genetic disorder caused by the partial or complete lack of an X chromosome. TS can cause a variety of medical and developmental conditions. We aimed to investigate TS mosaicism and variants pattern and research the presence of a correlation...

Descripción completa

Detalles Bibliográficos
Autores principales:	Farhud, Dariush, Asgarian, Rojiar, Seifalian, Amelia, Mostafaeinejad, Paria, Eslami, Maryam
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Tehran University of Medical Sciences 2021
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819239/ https://www.ncbi.nlm.nih.gov/pubmed/35223574 http://dx.doi.org/10.18502/ijph.v50i10.7507

Ejemplares similares

Genetic of Alzheimer’s Disease: A Narrative Review Article
por: KHANAHMADI, Mohammad, et al.
Publicado: (2015)

Turner syndrome and genetic polymorphism: a systematic review
por: de Marqui, Alessandra Bernadete Trovó
Publicado: (2015)

Combination of Genetics and Nanotechnology for Down Syndrome Modification: A Potential Hypothesis and Review of the Literature
por: TAFAZOLI, Alireza, et al.
Publicado: (2019)

Analysis of genetic variability in Turner syndrome linked to long-term clinical features
por: Suntharalingham, Jenifer P., et al.
Publicado: (2023)

Gjb3 Gene Mutations in Non-Syndromic Hearing Loss of Bloch, Kurd, and Turkmen Ethnicities in Iran
por: ALIAZAMI, Farnoush, et al.
Publicado: (2020)

Clinical and genetic characteristics in a group of 45 patients with Turner syndrome (monocentric study)
por: Bucerzan, Simona, et al.
Publicado: (2017)

Graves’ Disease in a Young Patient With Turner’s Syndrome: The Genetic Association
por: Majumder, Anirban, et al.
Publicado: (2023)

An Evidence-Based Systematic Review of Human Knee Post-Traumatic Osteoarthritis (PTOA): Timeline of Clinical Presentation and Disease Markers, Comparison of Knee Joint PTOA Models and Early Disease Implications
por: Khella, Christine M., et al.
Publicado: (2021)

Current controversies in turner syndrome: Genetic testing, assisted reproduction, and cardiovascular risks()
por: Ackermann, Amanda, et al.
Publicado: (2014)

Health Tract, No. 261: Boils
Publicado: (1866)

Nationwide Study of Turner Syndrome in Ukrainian Children: Prevalence, Genetic Variants and Phenotypic Features
por: Zelinska, Nataliya, et al.
Publicado: (2018)

Rare Association between Two Genetic Conditions: Turner Syndrome and Neurofibromatosis Type 1
por: El Qadiry, R., et al.
Publicado: (2022)

Turner syndrome and neurofibromatosis type 1: the unusual combination of two common genetic disorders
por: Vieira, Inês, et al.
Publicado: (2022)

Anti-Inflammatory Therapeutic Approaches to Prevent or Delay Post-Traumatic Osteoarthritis (PTOA) of the Knee Joint with a Focus on Sustained Delivery Approaches
por: Khella, Christine M., et al.
Publicado: (2021)

Health disparities in Turner Syndrome: UTHealth Turner Syndrome Research Registry
por: Donate, Priscille, et al.
Publicado: (2023)

Clinical and cytogenetic characteristics of patients diagnosed with Turner syndrome in a clinical genetics service: cross-sectional retrospective study
por: Nunes, Maurício Rouvel, et al.
Publicado: (2021)

A Case Report of Genetic Cascade Screening in Dilated Cardiomyopathy: A Perspective for Preventive Cardiology
por: Barati, Zeinab, et al.
Publicado: (2021)

TURNER'S SYNDROME WITH MANIA
por: Hebbar, Sudhir, et al.
Publicado: (1999)

Hyperthyroidism with Turner Syndrome
por: Artati, Ratna Dewi, et al.
Publicado: (2013)

Parsonage–Turner syndrome()
por: Monteiro dos Santos, Ricardo Barreto, et al.
Publicado: (2015)

Epigenetics in Turner syndrome
por: Álvarez-Nava, Francisco, et al.
Publicado: (2018)

Management of Turner Syndrome
por: Gawlik, Aneta
Publicado: (2015)

Parsonage-Turner Syndrome
por: Van Snick, Elyn, et al.
Publicado: (2023)

PMM no. 26.1 & 4.2
Publicado: (1981)

Mother’s Happiness with Cognitive - Executive Functions and Facial Emotional Recognition in School Children with Down Syndrome
por: MALMIR, Maryam, et al.
Publicado: (2015)

Turner Syndrome and the Risks of Clinical Depression in Adolescence
por: Gupta, Mayank, et al.
Publicado: (2021)

Dogmatism and Happiness
por: MALMIR, Maryam, et al.
Publicado: (2017)

Validation of auxological reference values for Japanese children with Noonan syndrome and comparison with growth in children with Turner syndrome
por: Isojima, Tsuyoshi, et al.
Publicado: (2017)

FRI261 A Case Of Cushing Syndrome And Hyperandrogenism Secondary To An Adrenal Cortical Oncocytoma
por: Hall, Elizabeth, et al.
Publicado: (2023)

Case Report: Genetic Analysis of a Small Supernumerary Marker Chromosome in a Unique Case of Mosaic Turner Syndrome
por: Li, Chao, et al.
Publicado: (2022)

Pancreatic mucinous cystic tumor in Turner syndrome: How a tumor bends to a genetic disease()
por: Pizzi, Marco, et al.
Publicado: (2013)

261. Adaptive Immunosuppression in Children with Septic Shock
por: Cruz Vidal, Diego A, et al.
Publicado: (2023)

Turner syndrome with primary hyperparathyroidism
por: Park, Jungmee, et al.
Publicado: (2013)

Endocrine autoimmunity in Turner syndrome
por: Grossi, Armando, et al.
Publicado: (2013)

Turner Syndrome with Ulcerative Colitis
por: Hyodo, Hiromi, et al.
Publicado: (2009)

Glucose Metabolism in Turner Syndrome
por: Sun, Lin, et al.
Publicado: (2019)

Metabolic Fingerprint of Turner Syndrome
por: Bugajska, Jolanta, et al.
Publicado: (2020)

Growth in girls with Turner syndrome
por: Isojima, Tsuyoshi, et al.
Publicado: (2023)

Cytogenetic evaluation of patients with clinical spectrum of Turner syndrome
por: Moka, Rajasekhar, et al.
Publicado: (2013)

Clinical phenotype and karyotype finding of Turner syndrome in Jakarta
por: Purwana, I Nyoman Arie, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_s1i95fgd31h4drn7cogidodqte