Cargando…

Otocephaly: A Case Report of a Rare Congenital Anomaly

Otocephaly is a rare congenital abnormality characterized by the absence or underdevelopment of the mandible, misplacement of the ears towards the front, a small mouth, and absence or underdevelopment of the tongue. The syndrome complex of otocephaly can be categorized into four types based on assoc...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ur Rahman, Hameed, Anees, Aleena, Ali, Muhammad Asfandiyar, Ahmad, Saad, Khan, Abu Baker
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cureus 2023
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10416669/ https://www.ncbi.nlm.nih.gov/pubmed/37575700 http://dx.doi.org/10.7759/cureus.41767

Ejemplares similares

Dengue Fever-Induced Hypokalemic Paralysis in a Pregnant Patient: An Uncommon Presentation of a Common Disease
por: Khan, Abu Baker, et al.
Publicado: (2023)

Otocephaly: Prenatal and postnatal imaging findings
por: Agarwal, Shalini, et al.
Publicado: (2011)

Agnathia-microstomia-synotia syndrome (otocephaly)
por: Díaz del Arco, Cristina, et al.
Publicado: (2020)

Cantrell Syndrome—A Rare Complex Congenital Anomaly: A Case Report and Literature Review
por: Mărginean, Claudiu, et al.
Publicado: (2018)

Agnathia-otocephaly complex diagnosed by prenatal ultrasound: a case report
por: Ji, Xueqin, et al.
Publicado: (2021)

Malrotated right supernumerary kidney: Case report of a rare anomaly
por: Al Dandan, Omran, et al.
Publicado: (2019)

Concurrence of Congenital Muscular Torticollis and Congenital Torticollis Due to Other Anomalies: Two Case Reports
por: Kim, Min-Wook, et al.
Publicado: (2021)

Case Report: Uterine Anomalies in Girls With a Congenital Solitary Functioning Kidney
por: van Dam, Mark J. C. M., et al.
Publicado: (2021)

Prenatal Diagnosis of Isolated Agnathia-Otocephaly: A Case Report and Review of the Literature
por: Kajiwara, Kazuhiro, et al.
Publicado: (2016)

Case Report: Congenital Perineal Lipoma Associated With Additional External Genitalia Anomalies
por: Tocchioni, Francesca, et al.
Publicado: (2022)

Expanding the spectrum of SMAD3‐related phenotypes to agnathia‐otocephaly
por: Meier, Nicole, et al.
Publicado: (2020)

Data Quality Assessment on Congenital Anomalies in Ontario, Canada
por: Miao, Qun, et al.
Publicado: (2020)

A de novo variant in OTX2 in a lamb with otocephaly
por: Paris, Julia Maria, et al.
Publicado: (2020)

Scrotoschisis: An extremely rare scrotal wall anomaly
por: Eshiba, Ahmed, et al.
Publicado: (2022)

The Voice of Parents of Children With a Congenital Anomaly – A EUROlinkCAT Study
por: Holm, Kristina Garne, et al.
Publicado: (2021)

Congenital second branchial cleft anomalies in children: A report of 52 surgical cases, with emphasis on characteristic CT findings
por: Chen, Wei, et al.
Publicado: (2023)

The Role of Lung Function Testing in Newborn Infants With Congenital Thoracic Arterial Anomalies
por: Columbo, Claudia, et al.
Publicado: (2021)

Whole Exome Sequencing in a Population With Severe Congenital Anomalies of Kidney and Urinary Tract
por: Harris, Meredith, et al.
Publicado: (2022)

Isolated Agnathia-Otocephaly Complex Diagnosed Prenatally for Ex-Utero Intrapartum Treatment: A Case Report
por: Suemitsu, Tokumasa, et al.
Publicado: (2023)

Risk Assessment of Severe Congenital Anomalies of the Kidney and Urinary Tract (CAKUT): A Birth Cohort
por: Katsoufis, Chryso P., et al.
Publicado: (2019)

Editorial: Congenital anomalies: State of the art and the new paradigms for a precision public health approach
por: Khoshnood, Babak, et al.
Publicado: (2022)

Agnathia-Otocephaly Complex Due to a De Novo Deletion in the OTX2 Gene
por: Fabiani, Marco, et al.
Publicado: (2022)

Factors Associated With the Development of Chronic Kidney Disease in Children With Congenital Anomalies of the Kidney and Urinary Tract
por: Isert, Saskia, et al.
Publicado: (2020)

Epidemiology of Multiple Congenital Anomalies Before and After Implementation of a Nationwide Prenatal Screening Program in Denmark
por: Toxværd, Marlene E., et al.
Publicado: (2021)

Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary system
por: Allred, Erika T., et al.
Publicado: (2023)

A Predictive Model of Postnatal Surgical Intervention in Children With Prenatally Detected Congenital Anomalies of the Kidney and Urinary Tract
por: Vasconcelos, Mariana A., et al.
Publicado: (2019)

Rare Course of Bilateral Congenital Diaphragmatic Hernia Treated Thoracoscopically—Case Report
por: Toczewski, Krystian, et al.
Publicado: (2020)

Case Report: A Rare Cause of Stridor and Hoarseness in Infants—Congenital Laryngeal Web
por: Wang, Yanyan
Publicado: (2022)

Non-surgical Correction of Congenital Ear Anomalies: A Review of the Literature
por: Feijen, Michelle M.W., et al.
Publicado: (2020)

Multiple congenital anomalies and adverse developmental outcomes are associated with neonatal intensive care admission and unilateral hearing loss
por: Horrocks, Lucy M., et al.
Publicado: (2023)

Editorial: Pyeloplasties in challenging scenarios as redo procedures, congenital anatomical anomalies and infants: Where do we stand?
por: Sforza, Simone, et al.
Publicado: (2023)

Prevalence and associated factors of structural congenital anomalies in resource limited setting, 2023: a systematic review and meta-analysis
por: Geda, Yohannes Fikadu, et al.
Publicado: (2023)

Congenital Hypofibrinogenemia: Presentation of a Rare Coagulation Disorder
por: Acevedo Viales, Karol, et al.
Publicado: (2020)

Congenital anterior urethral diverticula with posterior urethral valve: A rare combination, case report()
por: Abebe, Hana, et al.
Publicado: (2020)

Performance of the ADAPT-Treated CardioCel® Scaffold in Pediatric Patients With Congenital Cardiac Anomalies: Medium to Long-Term Outcomes
por: Neethling, William, et al.
Publicado: (2020)

Ultrasonic Features of Uncommon Congenital Heterotopic Colon and Pancreas in the Neck: An Extremely Rare Case Report
por: Wei, Yingli, et al.
Publicado: (2021)

The Prevalence and Pattern of Congenital Anomalies Among Neonates Admitted in a Tertiary Care Hospital in the Andaman and Nicobar Islands: A Retrospective Study
por: Sravani, Tera, et al.
Publicado: (2023)

Sirenomelia- A rare congenital anomaly: Case report
por: Thombare, Dipanjali, et al.
Publicado: (2023)

Ectopic Crossed Testis: A Rare Anomaly of Testicular Migration
por: Nunna, Bhagyasri, et al.
Publicado: (2023)

Simulation Surgery Using 3D 3-layer Models for Congenital Anomaly
por: Ueda, Koichi, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_ea2qklg2l5bam3rvoch46tlcct