Articles
Proteus syndrome in children symptoms causes and treatment
Proteus Syndrome in Children is a very rare and inherited condition that affects the growth of blood vessels and tissues, leading to enlargement or deformities in different parts of a child’s body. This condition can cause significant concern for parents, especially if it is associated with...
MoreCongenital hypertrichosis in children symptoms causes and treatment
Congenital Hypertrichosis Lanuginosa, also known as Werewolf Syndrome in infants and children, is a very rare condition that causes excessive hair growth all over the body from birth. This condition may appear as thick hair covering the face, hands, or the entire body, which often makes parents...
MoreHarlequin Fish Disease in Infants Symptoms and Treatment
Harlequin ichthyosis in newborns is a rare and serious skin disorder that appears from the first day of life. Affected infants have very thick, scaly skin with deep cracks, which can impact the movement of the face and limbs.The main cause is a genetic mutation in the ABCA12 gene, and the condition ...
MoreSeth-Chotzen syndrome in children causes symptoms and treatment methods
Crouzon–Sutphen Syndrome is a rare genetic disorder that affects the development of bones and the face in children, causing noticeable changes in the shape of the skull and jaw. Although uncommon, early diagnosis and proper medical follow-up can significantly improve a child’s quality...
MoreCrouzon syndrome in children symptoms causes treatment and prevention
Crouzon syndrome is a rare genetic condition that affects the development of the skull and face in children. Children with this condition often show noticeable deformities in the shape of the head and facial structure, which can sometimes impact the eyes, teeth, jaw, and even breathing or hearing....
MoreWilliams syndrome in children symptoms diagnosis and complete treatment
Williams Syndrome in Children is a rare genetic condition that affects physical and cognitive development and can appear in the first months of a child’s life. Children with Williams Syndrome may have distinctive facial features, muscle weakness, and heart or behavioral issues. Early...
MoreMiller-Dieker Syndrome in Children Causes Risks and Treatment
Miller–Dieker syndrome is a rare genetic disorder that affects brain development and the nervous system. Many parents first notice delays in milestones or difficulties with movement and speech, then start looking for answers. In this Dalili Medical guide, we’ll walk you through the...
MoreSeborrheic Eczema in Infants Causes Symptoms and Treatment
Cradle cap (infantile seborrheic eczema) is one of the most common skin problems parents face during the first year of a baby’s life. It usually appears on the scalp in the form of yellow or white scales, leaving many mothers confused about whether to treat it naturally or with...
MoreBone deformities in children and infants causes types and methods of repair
Bone deformities in children and newborns are among the most concerning issues for parents, as they not only affect the child’s appearance but also impact their movement and normal growth. In some cases, these deformities are congenital, present from birth, while in other cases they develop...
MoreHablich syndrome in children symptoms diagnosis and comprehensive treatment
Happleich Syndrome in Children is one of the rare disorders that affect the skin, bones, and sometimes internal organs. Although it is uncommon, early diagnosis and careful medical follow-up can help reduce complications and improve the child’s quality of life.In this Dalili Medical article,...
MoreGlass Baby Syndrome in Children Symptoms Causes and Treatment
Osteogenesis imperfecta, also known as “brittle bone disease,” is a very rare genetic condition that affects the bones and the immune system. It makes children more prone to fractures and injuries even from minor pressure or falls.In this we will explore the causes of osteogenesis ...
MoreChediak-Higashi Syndrome in Children Stages Risks and Treatment
Chediak-Higashi Syndrome in children is a very rare condition that affects the immune system and vital body functions. It usually appears from birth or within the first few years of life, causing symptoms such as recurrent infections, skin and hair problems, and serious blood complications.In this...
MoreSeckel syndrome in children symptoms causes and early treatment
Cyclopia is an extremely rare condition that affects the development of the brain and face from the early stages of pregnancy. This syndrome presents with noticeable features such as fused eyes or a single eye in the center of the face, along with abnormalities in the nose and jaw, often leading to ...
MoreTreacher Collins Syndrome in Children Symptoms Causes and Treatment
Treacher Collins Syndrome in Children is a rare genetic condition that affects the development of the bones in the face and skull. Children with this syndrome often show noticeable facial differences, such as underdeveloped cheekbones, a small jaw, and problems with the ears and eyes. This...
MoreTypes of fetal and infant skull deformities during birth and their complications
Cranial deformities in newborns and infants during birth are rare medical conditions but very important to monitor early. These deformities can appear in different forms, such as flat head, skull asymmetry, or premature closure of skull sutures, and each type may lead to potential complications...
MoreParry-Romberg Syndrome in Children Symptoms and Complete Treatment
Parry-Romberg Syndrome in Children is a rare condition that affects the development of the face and underlying tissues. It usually appears as a gradual loss of facial muscles, skin, and sometimes bone on one side of the face. This condition can lead to health and cosmetic issues, as well as...
MoreRubinstein-Taybi Syndrome in Children Causes Symptoms and Treatment
Rubinstein-Taybi Syndrome is a rare genetic condition that appears in children and affects physical and mental development, as well as certain distinctive features. A child with this syndrome may show characteristic traits such as broad fingers, learning difficulties, and delays in speech or...
MoreGiant baby syndrome signs causes and treatment methods
Gigantism in children is a rare condition in which a child grows faster than normal due to excessive secretion of growth hormone before the growth plates close. This syndrome is characterized by noticeable symptoms such as enlarged hands and feet and distinctive facial features. If not diagnosed...
MoreVampire Girl Disease in Children Causes Symptoms and Treatment
This could be a sign of Congenital Erythropoietic Porphyria (CEP), also known as the “Vampire Child Disease.” CEP is a rare genetic condition that affects red blood cells and causes both skin and blood-related symptoms.In this guide, we’ll discuss the main causes, symptoms,...
MoreVanishing Twin Syndrome Signs Causes and Early Diagnosis
Pregnancy is a journey full of joy and expectations, but sometimes unexpected events occur, such as Vanishing Twin Syndrome (VTS), where one of the twins stops developing and is absorbed by the body. This condition is common during the early months of pregnancy and often causes anxiety for mothers, ...
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