Children diseases
Eczema in Infants: From Diagnosis to Treatment
Infant eczema, also known as atopic dermatitis, affects up to 25% of babies and can be distressing for both infants and parents. Early recognition and proper management are crucial for controlling symptoms and providing relief. This comprehensive guide explores the journey from diagnosis to treatment, helping parents understand and effectively manage their baby's eczema.
Children diseases
School-Age Children and Eczema: A Guide for Parents and Teachers
Managing eczema in school-age children requires a collaborative effort between parents, teachers, and healthcare providers. This comprehensive guide aims to help both parents and educators understand the challenges faced by children with eczema and provide practical solutions for supporting them in the school environment.
Children diseases
Baby Eczema: Signs, Symptoms, and Gentle Treatment Options
Watching your baby struggle with itchy, inflamed skin can be distressing for any parent. Baby eczema, also known as infantile atopic dermatitis, affects up to 25% of children, making it one of the most common skin conditions in infancy. This comprehensive guide will help you understand, identify, and gently manage your baby's eczema.
Children diseases
ARTX Syndrome: Understanding a Rare X-Linked Intellectual Disability
Understanding rare genetic conditions is crucial for healthcare providers and families alike. ARTX syndrome, also known as ATRX syndrome or Alpha-Thalassemia X-Linked Intellectual Disability syndrome, is a rare genetic condition that primarily affects males. This comprehensive guide explores the causes, symptoms, diagnosis, and management options for individuals living with ARTX syndrome.
Children diseases
Trisomy types, causes, symptoms, treatment, prevention, FAQs
Trisomy is a genetic disorder characterized by the presence of an extra chromosome in the cells of the body. This condition can lead to various developmental and medical complications, depending on the specific chromosome involved and the severity of the trisomy.
Children diseases
Edwards syndrome trisomy 18 causes, symptoms, diagnosis, treatment, screening, prevention, FAQ
Trisomy 18, also known as Edwards syndrome, named after the British physician John Hilton Edwards, who first described the condition in 1960, Â is a genetic condition characterized by the presence of an extra chromosome 18 in some or all of the body's cells.
Children diseases
Adams-Oliver Syndrome (AOS)
Adams-Oliver Syndrome (AOS) is a rare congenital disorder characterized by the combination of aplasia cutis congenita (ACC) and terminal transverse limb defects. Named after...
Children diseases
Prune belly syndrome
Prune Belly Syndrome (PBS), also known as Eagle-Barrett syndrome, is a rare congenital disorder characterized by a triad of abnormalities: deficient development of the...
Children diseases
Kawasaki Disease
Kawasaki disease is a rare condition that primarily affects children under the age of five. It is characterized by inflammation of the blood vessels...
Children diseases
Idiopathic thrombocytopenic purpura (ITP)
ITP or Idiopathic thrombocytopenic purpura as it is commonly called, is a condition characterized by low blood platelet counts. In order for the blood to...