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Adrenal Gland Disorders01:27

Adrenal Gland Disorders

Adrenal gland disorders manifest when the production of adrenal hormones deviates from the norm, resulting in either excessive or insufficient concentrations.
Adrenal insufficiency, characterized by insufficient cortisol and aldosterone production, leads to conditions like Addison's disease. This disorder, affecting the adrenal cortex, exhibits symptoms such as skin bronzing, dehydration, low blood pressure, fatigue, and weight loss. Congenital adrenal hyperplasia, a genetic ailment causing...
Nephrotic Syndrome I : Introduction01:24

Nephrotic Syndrome I : Introduction

Nephrotic Syndrome is a chronic kidney disorder defined by clinical findings such as severe proteinuria, hypoalbuminemia, hyperlipidemia, and edema. These symptoms result from damage to the glomeruli, the kidney’s filtering units, increasing their permeability to proteins.Definition and Meaning:Proteinuria, defined as the loss of more than 3.5 grams of protein per day in adults, is a crucial feature of nephrotic syndrome. This condition is often accompanied by edema, the accumulation of fluid...
Smooth Endoplasmic Reticulum01:21

Smooth Endoplasmic Reticulum

Smooth endoplasmic reticulum or smooth ER is a sub-organelle with specialized functions in animal cells and plant cells. It is often associated with the tubule morphology of the endoplasmic reticulum.
The ER provides optimal conditions for synthesizing steroid hormones and lipids, such as phospholipids and triglycerides. Traditionally, lipid metabolism was considered to be a smooth ER function. However, there is no direct evidence to prove that rough ER is completely excluded from lipid...
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...
Portal Hypertension01:22

Portal Hypertension

Portal hypertension is an increase in blood pressure within the portal venous system. Normally, this pressure is less than 5 mmHg. It is considered clinically significant when it rises above 10 mmHg. At this threshold, complications from altered blood flow and venous congestion emerge.EtiologyPortal hypertension arises from conditions that impede blood flow through the liver. The most common cause is cirrhosis, in which chronic liver injury leads to fibrotic scarring. This fibrosis narrows or...
Type IV Collagen of Basal Lamina01:05

Type IV Collagen of Basal Lamina

Type IV collagen is a 400 nm long, network-forming collagen that acts as a barrier between the epithelial and endothelial cells. Type IV collagen  forms the backbone of the basement membrane by scaffolding with laminin, entactin, proteoglycans, and fibronectin. Apart from rendering structural support to the basement membrane, it also helps entail signaling potentials necessary for both pathological and physiological functions.
A type IV collagen molecule has six alpha chains which can exist in...

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Related Experiment Video

Updated: May 21, 2026

Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome
06:48

Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome

Published on: March 23, 2022

Binder's syndrome.

Upendra Jain1, Gagan Thakur, Amitabh Kallury

  • 1Department of Orthodontia, People's College of Dental Sciences and Research Centre, Bhopal, Madhya Pradesh, India.

BMJ Case Reports
|June 8, 2012
PubMed
Summary

Binder syndrome, or maxillonasal dysplasia, is a rare developmental anomaly causing midfacial hypoplasia. This case report details a 16-year-old female with classical features and discusses a multidisciplinary treatment approach.

Area of Science:

  • Craniofacial development
  • Medical genetics
  • Pediatric dentistry

Background:

  • Binder syndrome, also known as maxillonasal dysplasia, is an uncommon congenital condition.
  • It primarily affects the anterior maxilla and nasal complex, leading to characteristic facial deformities.
  • Key features include midfacial hypoplasia, a short nose, flat nasal bridge, and malocclusion.

Observation:

  • A 16-year-old female presented with significant facial deformity.
  • Clinical examination revealed classical features consistent with maxillonasal dysplasia.
  • The patient exhibited midfacial underdevelopment and a class III malocclusion.

Findings:

  • The condition results from a failure of development in the premaxillary area.
  • Associated deformities involve the nasal skeleton and overlying soft tissues.

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  • Skeletal anomalies contribute to the characteristic flattened midface and dental issues.
  • Implications:

    • Early diagnosis of Binder syndrome is crucial for effective management.
    • A multidisciplinary approach involving orthodontics, surgery, and speech therapy is often required.
    • Comprehensive treatment aims to improve both functional and aesthetic outcomes in affected individuals.