Cargando…

Duplication of 19q (13.2-13.31) associated with comitant esotropia: A case report

BACKGROUND: Comitant esotropia is the most common form of strabismus. It is caused by heterogeneous environmental and genetic risk factors. The pure duplication of the long arm of chromosome 19 is a rare abnormality. Only 8 patients with partial trisomy of the long arm of chromosome 19q have been re...

Descripción completa

Detalles Bibliográficos
Autores principales:	Feng, Yue-Lan, Li, Ning-Dong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Baishideng Publishing Group Inc 2021
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281424/ https://www.ncbi.nlm.nih.gov/pubmed/34307605 http://dx.doi.org/10.12998/wjcc.v9.i20.5526

Ejemplares similares

Adult expression of a 3q13.31 microdeletion
por: Lowther, Chelsea, et al.
Publicado: (2014)

Duplication of subtelomeric regions in an adult with acute monocytic leukemia with an acquired jumping translocation involving 3q13.31-qter
por: Kjeldsen, Eigil
Publicado: (2017)

A rare 3q13.31 microdeletion including GAP43 and LSAMP genes
por: Gimelli, Stefania, et al.
Publicado: (2013)

LSAMP Rearrangement in Acute Myeloid Leukemia With a Jumping Translocation Involving 3q13.31
por: Yoon, Jung, et al.
Publicado: (2021)

A Pilot Study on Collective Effects of 22q13.31 Deletions on Gray Matter Concentration in Schizophrenia
por: Liu, Jingyu, et al.
Publicado: (2012)

Genetic susceptibility to hepatocellular carcinoma in chromosome 22q13.31, findings of a genome‐wide association study
por: Wang, Zhanwei, et al.
Publicado: (2021)

Identification of recurrent 3q13.31 chromosomal rearrangement indicates LSAMP as a tumor suppressor gene in neuroblastoma
por: Martinez-Monleon, Angela, et al.
Publicado: (2023)

A locus at 19q13.31 significantly reduces the ApoE ε4 risk for Alzheimer’s Disease in African Ancestry
por: Rajabli, Farid, et al.
Publicado: (2022)

Acute Acquired Comitant Esotropia in Adults: Is It Neurologic or Not?
por: Erkan Turan, Kadriye, et al.
Publicado: (2016)

Management of acute acquired comitant esotropia in children
por: Dragomir, Mihaela Sorina, et al.
Publicado: (2023)

Neurological pathologies in acute acquired comitant esotropia
por: Nouraeinejad, Ali
Publicado: (2023)

A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3
por: Addis, L, et al.
Publicado: (2010)

Surgical outcomes of acute acquired comitant esotropia of adulthood
por: Kim, Dae Hyun, et al.
Publicado: (2021)

The Effects of Divalent Cation-Chelated Prion Fibrils on the Immune Response of EOC 13.31 Microglia Cells
por: Jen, Huan-I, et al.
Publicado: (2020)

Spontaneous late-onset comitant acute nonaccommodative esotropia in children
por: Naik, Uday V, et al.
Publicado: (2008)

Acute Comitant Esotropia in a Child With a Cerebellar Tumor
por: Lee, Jong-Min, et al.
Publicado: (2009)

Acute acquired comitant esotropia related to excessive Smartphone use
por: Lee, Hyo Seok, et al.
Publicado: (2016)

Clinical features of acute acquired comitant esotropia in the Chinese populations
por: Fu, Tao, et al.
Publicado: (2017)

Clinical characteristics and surgical outcomes of acute acquired Comitant Esotropia
por: Cai, Chunyan, et al.
Publicado: (2019)

Acute Acquired Comitant Esotropia: Etiology, Clinical Course, and Management
por: Lekskul, Apatsa, et al.
Publicado: (2021)

Possibility of Neurological Diseases Associated with Acute Acquired Comitant Esotropia
por: Montriwet, Mayuree
Publicado: (2023)

A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features
por: Molin, A-M, et al.
Publicado: (2011)

Inherited Xq13.2-q21.31 duplication in a boy with recurrent seizures and pubertal gynecomastia: Clinical, chromosomal and aCGH characterization
por: Linhares, Natália D., et al.
Publicado: (2016)

A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous family
por: Belhedi, Nejla, et al.
Publicado: (2013)

Mosaic 15q duplication syndrome (tetrasomy 15q11.1-q13.2) in a child with behavior disorders: case report
por: Rodrigues, Maurício A., et al.
Publicado: (2019)

Spontaneous late-onset comitant acute non-accommodative esotropia in children
por: Pandey, Pramod Kumar, et al.
Publicado: (2008)

Varied aetiology of acute acquired comitant esotropia: A case series
por: Kemmanu, Vasudha, et al.
Publicado: (2012)

19q12q13.2 duplication syndrome: neuropsychiatric long-term follow-up of a new case and literature update
por: Nacinovich, Renata, et al.
Publicado: (2017)

Chromosome 13q deletion syndrome involving 13q31-qter: A case report
por: Wang, Yue-Ping, et al.
Publicado: (2017)

Non-adjustable surgery for acute acquired comitant esotropia under general anesthesia
por: Lim, Soo Hyun, et al.
Publicado: (2022)

Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability
por: Mehvari, Sepideh, et al.
Publicado: (2020)

Botulinum Toxin Injection versus Extraocular Muscle Surgery for Acute Acquired Comitant Esotropia
por: Suwannaraj, Sirinya, et al.
Publicado: (2023)

The efficacy of botulinum toxin type A treatment and surgery for acute acquired comitant esotropia
por: Li, Yipao, et al.
Publicado: (2023)

A Case Report of Nystagmus with Acute Comitant Esotropia Secondary to Heroin Withdrawal: A Novel Presentation
por: Rabin, Richard L.
Publicado: (2015)

Acute comitant esotropia in a very young child due to combined mechanism: A case report
por: Fathima, Allapitchai, et al.
Publicado: (2020)

Case Report: A Paternal 20q13.2-q13.32 Deletion Patient With Growth Retardation Improved by Growth Hormone
por: Liu, Yu, et al.
Publicado: (2022)

Duplications at 19q13.33 in patients with neurodevelopmental disorders
por: Pérez-Palma, Eduardo, et al.
Publicado: (2018)

Autistic disorder associated with a paternally derived unbalanced translocation leading to duplication of chromosome 15pter-q13.2: a case report
por: Wu, David J, et al.
Publicado: (2009)

Two Pediatric Patients with Acute Acquired Comitant Esotropia as the First Symptom of Brainstem Tumor: A Case Report
por: Yagasaki, Ayaka, et al.
Publicado: (2023)

Management of idiopathic intracranial hypertension in an infant with bilateral congenital cataract and associated comitant sensory esotropia
por: Matalia, Jyoti Himanshu, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_u5q9r47aqmt5mhau1i3nhp7bh4