Articles

DiGeorge Syndrome in Children and Infants Symptoms and Treatment

DiGeorge Syndrome is one of the rare genetic disorders that appear in infants and children due to a problem in chromosome 22. This condition can cause heart defects, weakened immunity, and delayed growth and speech. That’s why early detection is very important to start the right treatment. In ...

Kwashiorkor in Children Causes Symptoms and Best Treatments

Kwashiorkor in children is considered one of the most dangerous forms of malnutrition, as it directly affects a child’s growth and immune health. Children with this condition often experience symptoms such as swollen abdomen and limbs, muscle wasting, weakened immunity, and changes in hair...

Masturbation in children causes ages and how to deal with it safely

The topic of young children and infants engaging in masturbation often makes many parents anxious and unsure. The truth is, a child touching their genitals is sometimes a normal behavior and part of their natural curiosity as they explore their own body. However, it can become concerning if it...

Chagas syndrome in children symptoms treatment and advice for parents

Congenital (Hereditary) Chagas Syndrome in Children is a rare medical condition, but it can significantly impact a child’s health and physical and mental development. This condition usually occurs due to a genetic mutation or hereditary factors and can cause a range of distinctive symptoms,...

Lennox-Gastaut syndrome in children symptoms treatment and advice

Lennox-Gastaut Syndrome (LGS) is one of the most severe forms of childhood epilepsy, usually appearing between the ages of 3 and 5. A child with LGS experiences frequent and multiple types of seizures that affect daily life, along with delays in cognitive and motor development. In this Dely Medical ...

Plum belly syndrome in children causes symptoms and treatment

Prune Belly Syndrome in children is a very rare condition, but it can cause significant concern for parents, especially when they notice weak abdominal muscles and a protruding, sagging belly. The condition doesn’t just affect the appearance of the abdomen—it can also lead to kidney and ...

Transparent belly syndrome in children causes symptoms and treatment methods

Transparent Abdomen Syndrome in children is one of the very rare medical conditions that often causes parents great concern when they notice it. In this condition, the abdominal wall is unusually thin or transparent, making the internal organs clearly visible. Although this syndrome is not as...

Watson syndrome in children symptoms causes and treatment

These signs may be an indication of Watson syndrome in children, a rare genetic condition that can be managed with proper care. Early monitoring plays a key role in protecting your child’s health.In this Dalily Medical article, we will explore together the causes of the syndrome, its main...

Cushing s syndrome in children symptoms causes and modern treatment methods

Cushing’s syndrome in children is a rare condition that affects the body’s hormones and growth, causing symptoms such as rapid weight gain, facial swelling, and problems with growth and bones. Understanding the causes, symptoms, early diagnosis, and treatment is essential for parents to ...

Brocade syndrome in children causes symptoms and treatment methods

Bruck syndrome in children is a rare genetic condition that affects the growth of bones and joints, causing issues such as short stature and deformities in the hands or feet. Understanding its causes, symptoms, and early diagnostic methods helps parents monitor their children properly, reduce...

Fanconi Anemia in Children is a rare genetic disorder, but it has a significant impact on a child’s health and daily life. The disease affects the bone marrow and the body’s ability to produce healthy blood cells, leading to issues such as persistent fatigue, easy bruising, and an...

Wyvern syndrome in children causes symptoms and modern treatment methods

Weaver Syndrome is a rare genetic disorder that affects children, characterized by rapid growth, distinctive facial features, and sometimes delays in motor and cognitive skills. Despite its rarity, early recognition of the symptoms and causes plays a crucial role in improving the child’s...

Stargardt syndrome in children causes symptoms and treatment methods

Stargardt Disease in Children (Stargardt Disease) is a rare inherited condition that affects the retina, leading to a gradual loss of central vision, while peripheral (side) vision usually remains intact. Although the disease does not impact intelligence, it can make tasks like reading and...

Triatrial septal defect syndrome in children symptoms causes and treatment

Cor Triatriatum in Children is one of the most serious congenital heart defects, directly affecting blood flow within the child’s heart and the amount of oxygen delivered to the body. Infants with this condition may show symptoms such as cyanosis (bluish skin), breathing difficulties, and...

Eisenmenger syndrome in children signs causes and treatment options

Eisenmenger Syndrome is one of the most serious congenital heart defects in children. It develops when an untreated heart defect causes severe pulmonary hypertension (high blood pressure in the lungs), leading to a reversal of blood flow inside the heart. This condition directly affects a...

Hypoplastic left heart syndrome in children symptoms and treatment

Hypoplastic Left Heart Syndrome (HLHS) in Children is one of the most serious congenital heart diseases, affecting the heart’s ability to pump blood to the rest of the body. Children with this condition may experience breathing difficulties, feeding problems, poor growth, and require urgent...

Cardiovascular syndrome in children symptoms causes and treatment

Cardiovascular syndrome in children is a rare health condition that affects the heart and blood vessels, and it can lead to serious health problems if not detected early. In this  we will discuss the causes of the syndrome, its early symptoms, precise diagnostic methods, types of treatment...

Wilson s disease in children symptoms causes and easy treatment

Wilson’s Disease in Children is a rare genetic disorder that causes copper to accumulate in the liver, brain, and eyes, potentially leading to serious health problems if not detected and treated early. In this article on Dalili Medical, we explain the causes of Wilson’s disease, its...

Alagille syndrome in children the most important symptoms causes and treatment options.

Alagille Syndrome is a rare genetic disorder that affects children, primarily impacting the liver, heart, bones, and eyes. This syndrome is characterized by a wide range of symptoms that may appear at birth or during the early years of a child’s life, making early recognition crucial for...

Dravet Syndrome in Children Early Symptoms and How to Detect It

Dravet syndrome is a rare condition that affects infants and young children. It is mainly characterized by severe and recurrent seizures that usually begin during the child’s first year of life. Beyond seizures, children with Dravet syndrome may also experience delayed speech, learning...