Pyogenic liver abscess and peri ...
Papillon–Lefevre syndrome (PLS) is an autosomal recessive disease that is characterized by symmetric palmoplantar keratodermatitis and severe period ...
Shock: an unusual presentation ...
Kawasaki disease (KD) is a common acute systemic vasculitis of childhood. Although KD has wide spectrum of clinical features, shock is not one of it ...
Focal nodular hyperplasia of th ...
Focal nodular hyperplasia (FNH) is a benign hepatic lesion very rarely described in the pediatric population. It has been reported more frequently i ...
Spinal epidural abscess in a yo ...
Spinal epidural abscess (SEA) is a rare infection associated with well-established risk factors mainly in adults. We describe an 11-year-old girl wi ...
A child with mental retardation ...
A 5-year-old male child presented with progressively increasing asymmetrical overgrowth of limbs, hyperpigmentation on the right half of the body, a ...
Painful ulcers in a 5-year-old ...
A 5-year-old girl was admitted to our clinic with several painful ulcers spreading from the right elbow to the armpit. The right axillary lymph node ...
Clinical practice The bleeding ...
Mucocutaneous bleeding is common in childhood and may be the result of primary hemostatic disorders such as vascular abnormalities, von Willebrand d ...
Anorectal mucinous adenocarcino ...
Colorectal cancer is extremely rare in children with incidence of one child per one million. We report an 11-year-old boy who presented with a 3-mon ...
Subcutaneous fat necrosis in ne ...
Subcutaneous fat necrosis (SCFN) of the newborn is an uncommon, self-limiting panniculitis mostly occurring within the first few weeks after birth. ...
EGFR expression in acquired mid ...
Middle ear cholesteatomas are characterized by the presence of keratinized stratified squamous epithelium inside this cavity. It is considered to be ...
The effects of detraining on bl ...
The present study examined the change to clarify the effects of detraining on the concentration of lipid profiles, serum adipokines and antioxidant ...
Familial hypocalciuric hypercal ...
Familial hypocalciuric hypercalcemia is an uncommon cause of hypercalcemia that arises from mutations in the calcium-sensing receptor gene. Inactiva ...
Somatic symptoms, severe mood d ...
Many researchers have studied somatic symptoms in children. However, its association with severe mood dysregulation (SMD) is poorly known. The aim o ...
Effects of APOA5 S19W polymorph ...
Apolipoprotein (Apo) A5 is a protein involved in the activation of lipoprotein lipase (LPL) and the metabolism of triglyceride (TG)-rich lipoprotein ...
Bartter syndrome in two sisters ...
This article describes two sisters with type III Bartter syndrome (BS) due to a novel missense variant of the CLCNKB gene. The phenotypic expression ...
Lipoprotein lipase gene polymor ...
Childhood obesity is increasingly prevalent in the community and is related to many adult diseases. Lipoprotein lipase (LPL) plays a central role in ...
Risk factors of obesity in pres ...
To assess risk factors of childhood obesity, we carried out a case–control study in ten kindergartens in Changsha, the capital city in the Chinese p ...
4q34.1–q35.2 deletion in a boy ...
Small terminal or interstitial deletions involving bands 4q34 and 4q35 have been described in several patients with a relatively mild phenotype such ...
Pediatric tick-borne infections ...
Tick-borne encephalitis (TBE) and neuroborreliosis (NB) are well-known central nervous system (CNS) infections in children. Childhood tick-borne CNS ...
Relationship between symptoms o ...
This study examined the relationship between family functioning and attention-deficit/hyperactivity disorder (ADHD) symptoms in an Australian commun ...
Usefulness of wireless capsule ...
Inflammatory bowel disease (IBD) is a cause of chronic intestinal inflammation in children. In a subset of patients affected by IBD, arthropathy may ...
Pyruvate administered to newbor ...
Based on previous studies, we had made a try to administer sodium pyruvate to newborn Wistar rats suffering repetitive and profound hypoglycemia, wh ...
Isolated congenital tracheal st ...
Severe tracheal stenosis, resulting in functional atresia of the trachea is a rare congenital malformation with an estimated occurrence of two in 10 ...
End-stage renal disease in Slov ...
The aim of this study was to examine the occurrence of end-stage renal disease (ESRD) in Slovak children, to compare it with earlier Slovak data and ...
Gray hair and acrodermatitis en ...
Presentation of cystic fibrosis (CF) with an acrodermatitis enteropathica-like skin rash, anemia, and hypoproteinemia without pulmonary disease is r ...