Isolated congenital tracheal stenosis in a preterm newb ...
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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 ...
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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 ...
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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 ...
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Relationship between symptoms o ...
This study examined the relationship between family functioning and attention-deficit/hyperactivity disorder (ADHD) symptoms in an Australian commun ...
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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 ...
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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 ...
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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 ...
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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 ...
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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 ...
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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 ...
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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 ...
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Familial hypocalciuric hypercal ...
Familial hypocalciuric hypercalcemia is an uncommon cause of hypercalcemia that arises from mutations in the calcium-sensing receptor gene. Inactiva ...
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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 ...
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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 ...
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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. ...
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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 ...
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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 ...
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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 ...
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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 ...
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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 ...
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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 ...
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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 ...
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Pyogenic liver abscess and peri ...
Papillon–Lefevre syndrome (PLS) is an autosomal recessive disease that is characterized by symmetric palmoplantar keratodermatitis and severe period ...
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A young boy with diffuse hyperp ...
An 18-year-old male patient had presented with diffuse hyperpigmentation after birth and with adrenal insufficiency syndrome since childhood. After ...
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A boy with a one-sided red rash
We report on a boywith a sudden onset of unilateral skin lesions following tonsillar infection with fever 2 weeks before. The lesions consisted of e ...
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