Articles

Alien Hand Syndrome in Children Symptoms Causes and Effective Treatment

Have you ever noticed your child’s hand moving strangely without their control? Or making unexpected movements that confuse or frustrate them? This could be a sign of Alien Hand Syndrome (AHS) in children, a rare condition where the hand seems to act independently of the child’s will....

Stone girl disease in children symptoms causes and treatment

Have you ever noticed that your child has unusual joint stiffness or hard lumps in the muscles? Or maybe they were born with deformities in the thumbs or toes? These could be signs of Fibrodysplasia Ossificans Progressiva (FOP), also known as Stone Man Syndrome, a very rare condition where muscles, ...

Progeria in newborns causes symptoms and treatment

Have you ever noticed that your newborn seems to show signs of aging unusually fast? Or that their skin is extremely thin and their bones are fragile? This could be a sign of progeria in newborns, also known as premature aging. This condition is very rare and significantly affects a child’s...

Werewolf syndrome in children causes and treatment

Have you ever noticed your child showing unusual hair growth in unexpected areas? Or behaving in a way that seems strange or different? This could be a sign of Wolf Child Syndrome, a rare condition in children that sometimes affects both hair growth and behavior. In this Dalili Medical article,...

Alice in Wonderland Syndrome Signs Symptoms and Treatment in Children

Does your child sometimes see objects as unusually big or small? Or feel that their body doesn’t match the space around them? This could be a sign of Alice in Wonderland Syndrome (AIWS) in children, a rare condition that affects a child’s perception of their body, surroundings, and...

Tree Man Syndrome in Children Causes Symptoms and Treatment

Has your child started developing large, rough warts on their hands, feet, or other parts of the body, and seem to be easily affected with no clear reason? This could be a sign of Tree Man Syndrome in children, a very rare condition that causes the skin to grow warts resembling tree roots due to a...

Butterfly disease in children causes prevention methods and effective treatment

Is your child very sensitive? Even the slightest touch can hurt their skin and cause blisters or wounds? This is what happens with children who have Butterfly Disease, also known by doctors as Epidermolysis Bullosa. It’s a rare genetic condition that makes the skin extremely fragile, so even...

Huntington s disease in children risks early signs and the latest treatment methods

Huntington’s disease in children is a rare and complex genetic disorder that affects the nervous system and shows symptoms at an early age. Early detection helps parents and doctors manage the condition more effectively, reduce complications, and improve the child’s quality of...

Cohen syndrome in children warning signs best treatment methods and support

Have you noticed any delays in your child’s growth or difficulties with speech and walking? The reason could be Cohen Syndrome, a rare genetic condition that affects both the physical and mental development of children. In this Dalili Medical article, we will cover in detail: The...

Children and Usher Syndrome Types Symptoms and Modern Treatment Options

Have you noticed any hearing or vision problems in your child? It could be due to Usher Syndrome, a rare genetic condition that affects both hearing and sight. This article from Dalily Medical will help you understand everything about the condition: from early symptoms and types of the syndrome to...

Rare metabolic disorders in children causes symptoms and treatment

Have you ever heard of rare metabolic disorders in children? These are a group of genetic conditions where the body has trouble breaking down sugars, proteins, or fats. The result can lead to growth problems, delayed development, or even serious complications if not treated early. In this...

Scleroderma in children the most important symptoms causes and treatment

Childhood scleroderma is a rare condition that affects the skin and, in some cases, the joints and internal organs. Early detection of signs and symptoms helps parents and doctors intervene promptly, reducing complications and protecting the child’s health. In this  Dalily Medical...

Alport syndrome in children symptoms complications and treatment methods

Alport syndrome in children is a rare genetic disorder that affects the kidneys, hearing, and sometimes the eyes. Early awareness of the signs by parents enables prompt diagnosis and proper medical follow-up, which helps reduce complications and protects the child’s long-term health. we will...

Liver cirrhosis in children and infants symptoms causes and effective treatment methods

Pediatric liver fibrosis is a rare but serious condition that can significantly affect a child’s life if not detected early. This disease occurs due to the accumulation of fibrous tissue in the liver, often caused by genetic defects or problems in liver development during pregnancy, which can ...

Metabolic diseases in infants the most important causes and rapid treatment

Metabolic disorders in infants are among the most serious health issues that can affect children in their first months of life, as they impact the body’s ability to convert food into essential energy for growth. They often occur due to genetic enzyme deficiencies and usually appear through...

Ataxia in children types of the disease early signs and the latest treatment methods

Ataxia in children is a neurological condition that can cause significant concern for parents, especially when the child starts experiencing problems with balance and movement. This disorder affects muscle coordination and the ability to walk and move normally, and it can be either hereditary or...

Shaken Baby Syndrome Causes Symptoms and Treatment

Shaken Baby Syndrome (SBS) is one of the most severe injuries a child can experience during their early years. It occurs when an infant is shaken violently, whether intentionally or unintentionally. The danger lies in the direct impact on the brain and nervous system, which can lead to serious...

Legionnaires disease in infants symptoms causes and prevention

Legionellosis in infants is a rare but very serious condition that affects newborns and premature babies due to exposure to Legionella bacteria. Infected children often show severe lethargy, refusal to feed, coughing, and difficulty breathing. In severe cases, organ failure or life-threatening...

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Causes of sepsis in newborns and how to prevent and treat it

Neonatal sepsis is a critical and serious medical condition that affects newborns in their first days of life, posing a direct threat to their health and survival. Many parents may mistake common newborn signs, such as lethargy or refusal to feed, as minor issues. However, any delay in diagnosing...