Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Barrett Esophagus-II: Clinical Manifestations and Management01:21

Barrett Esophagus-II: Clinical Manifestations and Management

Individuals with Barrett's esophagus are often asymptomatic, but they may experience symptoms commonly associated with GERD, such as heartburn and acid regurgitation. Additional symptoms can include difficulty swallowing, chest pain, unintentional weight loss, blood in the stool (which may appear black, tarry, or bloody), and episodes of vomiting.
To diagnose Barrett's esophagus, healthcare providers often recommend an endoscopy for those showing symptoms of acid reflux. The procedure entails...
Methods of Documentation II: POMR01:26

Methods of Documentation II: POMR

The Problem-Oriented Medical Record (POMR) revolutionized medical record-keeping by introducing a systematic approach focusing on the patient's problems rather than merely listing symptoms. Dr. Lawrence Weed's introduction of this method in the 1960s marked a significant advancement in medical documentation. The POMR framework consists of four key components: the database, problem list, plan of care, and progress notes.
Sex-linked Disorders01:43

Sex-linked Disorders

Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
Cushing Syndrome I: Introduction01:26

Cushing Syndrome I: Introduction

Cushing syndrome refers to the collection of clinical manifestations that arise when tissues are exposed to excessive amounts of cortisol or cortisol-like medications over an extended period. Cortisol, a glucocorticoid produced by the adrenal cortex, regulates metabolism, immune responses, and the body’s adaptation to stress. When its concentration remains chronically elevated, these physiological pathways become dysregulated, resulting in the characteristic features of the syndrome.Exogenous...
Aneurysm II: Clinical Manifestations and Diagnostic Studies01:21

Aneurysm II: Clinical Manifestations and Diagnostic Studies

Thoracic, aortic arch and abdominal aneurysms are significant vascular conditions that can present with various clinical manifestations and lead to serious complications. Understanding these manifestations and the appropriate diagnostic studies is essential for effective management and treatment.Thoracic Aortic AneurysmsThoracic aortic aneurysms often remain asymptomatic until they reach a size that impinges on adjacent structures. They typically cause deep, diffuse chest pain that radiates to...
Cushing Syndrome II: Pathophysiology01:19

Cushing Syndrome II: Pathophysiology

Cortisol production is normally governed by the hypothalamic–pituitary–adrenal (HPA) axis, which maintains hormonal balance through tightly regulated feedback mechanisms. Disruption of this regulatory system is central to the development of Cushing syndrome, whether the excess cortisol originates from external medications or internal pathology. Persistent cortisol elevation alters metabolism, immune function, and endocrine signaling, producing the characteristic clinical features of the...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Factors affecting pain experience after lower third molar germectomy in teenagers-a clinical study.

European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry·2024
Same author

The Urbino Charter: a Declaration for the well-being of working people.

La Clinica terapeutica·2023
Same author

Retraction Note: Epidemiological characteristic of Orofacial clefts and its associated congenital anomalies: retrospective study.

BMC oral health·2023
Same author

Evaluation of dental demands and needs of people experiencing homelessness in the city of Rome, Italy.

European review for medical and pharmacological sciences·2022
Same author

Prevalence of molar incisor hypomineralization among school children in Rome, Italy.

Scientific reports·2022
Same author

The cornea as a reference point in orthodontic diagnosing, a retrospective study.

La Clinica terapeutica·2022

Related Experiment Video

Updated: Jun 10, 2026

Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas
07:00

Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas

Published on: February 28, 2019

Noonan syndrome: A case report.

G Ierardo1, V Luzzi, F Panetta

  • 1Sapienza University of Rome, Italy, Department of Paediatric Dentistry.

European Journal of Paediatric Dentistry
|July 20, 2010
PubMed
Summary
This summary is machine-generated.

Noonan syndrome, a genetic disorder on chromosome 12, presents with various systemic issues. Early orthodontic intervention with functional appliances can address dental and facial asymmetry in affected children.

Related Experiment Videos

Last Updated: Jun 10, 2026

Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas
07:00

Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas

Published on: February 28, 2019

Area of Science:

  • Genetics
  • Pediatrics
  • Orthodontics

Background:

  • Noonan syndrome is a rare genetic disorder caused by alterations in genes, with the primary gene located on chromosome 12.
  • This condition can manifest with a range of systemic complications affecting multiple organ systems.

Observation:

  • A case study involved an eight-year-old Caucasian girl diagnosed with Noonan syndrome.
  • The patient presented with otitis, cardiac issues, speech difficulties, lower limb asymmetry, and mild cognitive delay.
  • A notable habit of lower lip sucking was also observed.

Findings:

  • The diagnostic evaluation confirmed Noonan syndrome.
  • The patient exhibited characteristic systemic and developmental features associated with the condition.

Implications:

  • This case highlights the importance of early diagnosis and multidisciplinary management for Noonan syndrome.
  • Orthodontic treatment, including tooth extraction, molar sealing, and functional appliance use, was initiated to manage dental and facial irregularities.
  • Addressing such issues can potentially improve quality of life for individuals with Noonan syndrome.