Latest Updates
-
Purported Video of Muslim Mob Lynching & Hanging Hindu Youth In Bangladesh Shocks Internet -
A Hotel on Wheels: Bihar Rolls Out Its First Luxury Caravan Buses -
Bharti Singh-Haarsh Limbachiyaa Welcome Second Child, Gender: Couple Welcome Their Second Baby, Duo Overjoyed - Report | Bharti Singh Gives Birth To Second Baby Boy | Gender Of Bharti Singh Haarsh Limbachiyaa Second Baby -
Bharti Singh Welcomes Second Son: Joyous News for the Comedian and Her Family -
Gold & Silver Rates Today in India: 22K, 24K, 18K & MCX Prices Fall After Continuous Rally; Check Latest Gold Rates in Chennai, Mumbai, Bangalore, Hyderabad, Ahmedabad & Other Cities on 19 December -
Nick Jonas Dancing to Dhurandhar’s “Shararat” Song Goes Viral -
From Consciousness To Cosmos: Understanding Reality Through The Vedic Lens -
The Sunscreen Confusion: Expert Explains How to Choose What Actually Works in Indian Weather -
On Goa Liberation Day 2025, A Look At How Freedom Shaped Goa Into A Celebrity-Favourite Retreat -
Daily Horoscope, Dec 19, 2025: Libra to Pisces; Astrological Prediction for all Zodiac Signs
Laurence-Moon Syndrome (LMS) - Rare Genetic Disorder | Symptoms, Diagnosis, and Treatment
Laurence-Moon Syndrome (LMS) is a rare genetic disorder that affects multiple systems in the body. It is characterized by various physical and intellectual disabilities, including vision problems, obesity, developmental delays, and learning difficulties.

Causes of Laurence-Moon Syndrome
LMS is caused by mutations in specific genes involved in the development and functioning of cilia - tiny hair-like structures found on the surface of cells.
These mutations disrupt the normal structure and function of cilia, leading to the wide range of symptoms observed in individuals with LMS.
Effects of Laurence-Moon Syndrome
The effects of LMS can vary widely among affected individuals. One common feature is retinal degeneration, which leads to progressive vision loss or blindness.
Other effects may include hormonal imbalances resulting in obesity, motor coordination difficulties, intellectual disability, speech impairments, and delayed puberty.
Diagnosis and Treatment Options
Diagnosing LMS involves a thorough evaluation of an individual's medical history, physical examination, genetic testing for known mutations associated with LMS, as well as specialized tests such as electroretinography (ERG) to assess retinal function.
Currently, there is no cure for LMS; treatment focuses on managing symptoms and providing supportive care tailored to each individual's needs.
Managing Symptoms
Treatment approaches for LMS may include regular monitoring of vision and the use of visual aids, such as glasses or contact lenses. Hormonal imbalances can be managed with medications or hormone replacement therapy.
Physical and occupational therapies can help improve motor skills and coordination, while special education programs can support learning difficulties and intellectual disabilities.
Supportive Care
Individuals with LMS often require ongoing care from a team of healthcare professionals, including ophthalmologists, endocrinologists, geneticists, neurologists, psychologists, and educators. Regular check-ups are essential to monitor the progression of symptoms and adjust treatment plans accordingly.
Emotional support and counselling are also crucial for individuals with LMS and their families.



Click it and Unblock the Notifications











