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Related Concept Videos

Flail Chest-I01:24

Flail Chest-I

Overview of Flail Chest
Flail chest is a severe and potentially life-threatening condition characterized by the fracture of three or more adjacent ribs in multiple places. It is most commonly caused by direct impacts and trauma, such as motor vehicle accidents or injuries from a steering wheel impact. It can also occur due to falls in elderly individuals with osteoporosis, or assaults involving sharp objects.
Pathophysiology
The pathophysiology of flail chest is complex, involving fractures of...
Barrett Esophagus-I: Introduction01:21

Barrett Esophagus-I: Introduction

Barrett's esophagus is a medical condition where the esophageal mucosa is significantly damaged by stomach acid or other digestive fluids, often due to long-term exposure associated with gastroesophageal reflux disease (GERD). In GERD, a weakened or abnormally relaxed lower esophageal sphincter allows stomach acid to flow persistently into the esophagus.
This constant acid exposure transforms the esophagus's pink mucosal lining (stratified squamous epithelium) into a type of lining more similar...
Rheumatic Heart Disease I: Introduction01:23

Rheumatic Heart Disease I: Introduction

Rheumatic heart disease or RHD is a chronic condition that results from rheumatic fever, causing permanent damage to the heart valves.Etiology and Risk FactorsIt primarily arises from rheumatic fever, an inflammatory disease that can develop after untreated or inadequately treated group A streptococcal (GAS) pharyngitis. Streptococcus spreads through direct contact with oral or respiratory secretions. While the bacteria are the causative agents, factors like malnutrition, overcrowding, poor...
Rheumatic Heart Disease II: Clinical Manifestations and Diagnostic Studies01:22

Rheumatic Heart Disease II: Clinical Manifestations and Diagnostic Studies

The key clinical manifestations of Rheumatic heart disease (RHD) include several distinct cardiac symptoms.Carditis, a hallmark of acute rheumatic fever, involves inflammation of the heart's endocardium, myocardium, and pericardium. Chronic RHD often results from recurrent episodes of carditis. Its symptoms include the following:Murmurs are caused by valvular damage, especially to the mitral and aortic valves. Mitral stenosis or regurgitation is common, with characteristic heart murmurs...
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Positive Symptoms of Schizophrenia: Hallucinations and Delusions01:30

Positive Symptoms of Schizophrenia: Hallucinations and Delusions

Schizophrenia is a complex mental health disorder that can manifest with various positive symptoms, including thought, movement, and behavior disorders. These symptoms significantly disrupt cognitive and motor functions, leading to profound effects on an individual's ability to engage with the world.
Thought Disorders
Disorganized and unusual thought processes mark thought disorders in schizophrenia. One key feature is disorganized speech, where an individual's conversation includes loosely...

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Related Articles

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

Sort by
Same author

Xeroderma pigmentosum and keratoconus.

Documenta ophthalmologica. Advances in ophthalmology·1986
Same author

Ring melanoma of the iris. Iridocorneal endothelial syndrome.

International ophthalmology·1985
Same author

Meretoja syndrome. Lattice dystrophy of the cornea with hereditary generalized amyloidosis.

Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde·1979
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Melanoma of the conjunctiva [proceedings].

Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde·1977
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SLE syndrome with keratoconjunctivitis sicca, a side-effect of practolol [proceedings].

Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde·1977
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Malignant melanoma of the choroid.

Transactions of the ophthalmological societies of the United Kingdom·1973

Related Experiment Video

Updated: Jul 17, 2026

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment
07:26

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment

Published on: July 18, 2017

Hallermann-Streiff syndrome

P C Donders

    Documenta Ophthalmologica. Advances in Ophthalmology
    |September 30, 1977
    PubMed
    Summary

    This study details a rare syndrome distinct from mandibulo-facial dysostosis, presenting a case with ophthalmopathological examination for further understanding of this condition.

    Area of Science:

    • Ophthalmology
    • Genetics
    • Pathology

    Background:

    • The syndrome, distinct from Franceschetti's syndrome (mandibulo-facial dysostosis), was first recognized by Blodi and François in 1957 and 1958.
    • Despite approximately 60 reported cases, few have undergone histological study, highlighting a gap in understanding.

    Observation:

    • This report focuses on a specific case requiring detailed ophthalmopathological examination.
    • The examination aims to provide insights into the ocular manifestations and pathological characteristics of the syndrome.

    Findings:

    • The case report contributes valuable histological and ophthalmopathological data.
    • This data aids in differentiating the syndrome from similar genetic conditions.

    Implications:

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    • Further histological and ophthalmopathological studies are crucial for a comprehensive understanding of this rare syndrome.
    • Establishing distinct diagnostic criteria and potential therapeutic targets relies on such detailed case analyses.