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Neurodevelopmental Disorders

Understanding the Causes and Effects of Cornelia de Lange Syndrome

Introduction Cornelia de Lange Syndrome (CdLS) is a genetic disorder present from birth, but not always diagnosed at birth. Named after the Dutch pediatrician who...

Understanding the Complexities of Smith-Magenis Syndrome

Smith-Magenis syndrome (SMS) is a rare and complex genetic disorder that affects multiple organ systems of the body. It's characterized by a unique pattern...

Understanding Tuberous Sclerosis Complex: A Comprehensive Guide

Tuberous Sclerosis Complex (TSC) is a genetic disorder affecting multiple systems and causing non-cancerous tumors to grow in various parts of the body. These...

Unraveling the Complexities of Neurofibromatosis

Neurofibromatosis is a collection of three distinct genetic disorders that cause tumors to grow in the nervous system. These are neurofibromatosis type 1 (NF1),...

Understanding Prader-Willi Syndrome: Causes and Symptoms

Prader-Willi syndrome (PWS) is a highly complex genetic disorder affecting numerous parts of the body. Despite its considerable prevalence, it is not as well-known...

Understanding Williams Syndrome: Causes, Symptoms, and Management

Introduction Williams Syndrome (WS) is a rare genetic disorder that affects various systems in the human body, leaving a significant impact on one's growth, health,...

Understanding Angelman Syndrome: From Symptoms to Treatment

Angelman Syndrome is a complex genetic disorder that primarily affects the nervous system and presents a range of physical and developmental deficits. Named after...

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