Urticaria due to Urtica dioica ...
Urticaria is one of the most common dermatoses during the childhood, but it is very rare in the neonates. A 17-day-old infant with a generalized urt ...
Pediatric oncology for the gene ...
Since its establishment as a pediatric subspecialty oncology has become the near exclusive domain of specialized tertiary centers. This has greatly ...
Acquired nonscarring diffuse ha ...
A 3-year-old girl showed fine, sparse, and brittle scalp hair without signs of cicatricial cutaneous alterations. Dermoscopy as well as scanning ele ...
A novel WT1 gene mutation in a ...
Denys–Drash syndrome (DDS) is a rare genetic disorder featuring the triad ofWilms' tumor, early-onset renal failure, and 46, XY disorder of sex deve ...
A case report of hyperthyroid-a ...
We present the case of an 8-year-old boy with an anterior mediastinal mass and signs of hyperthyroidism. The anterior mediastinal mass had radiologi ...
N-carbamylglutamate treatment f ...
Hyperammonemia occurs mainly in patients with branched-chain organic acidemias such as propionic, methylmalonic, and isovaleric acidemias. Its patho ...
Early congenital syphilis in a ...
In the UK, diagnosis of syphilis among women of child-bearing age has more than doubled between 1999 and 2007, and each year, around ten cases of co ...
Ovarian cyst torsion in a patie ...
Congenital lipoid adrenal hyperplasia (CLAH) is the most severe form of congenital adrenal hyperplasia, characterized by lack of synthesis of all go ...
Household poisoning cases from ...
Mercury has a number of unique and fascinating properties. It is present in the environment in several forms, both organic and inorganic. Each of th ...
Dyggve–Melchior–Clausen syndrom ...
Dyggve–Melchior–Clausen (DMC) syndrome is a rare autosomal recessive disorder characterized by the association of a progressive spondyloepimetaphyse ...
Combination therapy for life-th ...
Premature infants with preterm premature rupture of membranes (PPROM) are at high risk of severe respiratory failure because of lung hypodysplasia a ...
Relevant factors influencing fl ...
The aim of this study was to discuss the influence of age, gender, obesity status, joint laxity, and the W-sitting habit on flatfoot in preschool-ag ...
Doppler manifestations of ducta ...
Patent ductus arteriosus in extremely premature babies is associated with major neonatal morbidities such as necrotizing enterocolitis and intravent ...
Destructive pulmonary staphyloc ...
Hyper IgE syndrome (HIES) is a rare primary immunodeficiency disorder, characterized by eczema, recurrent skin and lung infections, and significantl ...
Congenital acute lymphoblastic ...
Congenital leukemia is a rare disease with particular biological and clinical characteristics which differs from those of older children and adults. ...
Two siblings with triple A synd ...
The clinical and molecular data on triple A syndrome in two siblings (girl 3.5 years and boy 5.5 years at presentation) with early onset of neurolog ...
Nephrotic syndrome occurring du ...
Cystinuria is an autosomal recessive disorder characterized with abnormal tubular reabsorption of cystine and dibasic amino acids leading to cystine ...
Use of milrinone in the managem ...
Haemodynamic instability affects 22% to 29% of very low birth weight infants in the acute period following ligation of the ductus arteriosus and con ...
LEOPARD syndrome (PTPN11, T468M ...
Noonan syndrome (NS) and neurofibromatosis type 1 (NF1) are well-defined entities. The association of both disorders is called neurofibromatosis–Noo ...
Attention-deficit hyperactivity ...
The purpose of this study is to explore whether sustained exposure to vehicular air pollution affects the behavior and activities of children. The p ...
Cerebral hemiatrophy associated ...
The etiological relation of prolonged febrile seizures with hippocampal sclerosis and cerebral hemiatrophy is controversial. Causal relationship is ...
Fatal group A Streptococcus pur ...
Inhibition of tumor necrosis factor alpha (TNF-ل) is effective in the treatment of many pediatric autoimmune diseases and inflammatory conditions. C ...
de Quervain thyroiditis in a yo ...
de Quervain thyroiditis, also known as subacute thyroiditis, is a self-limited inflammatory disease of the thyroid gland. It is extremely rare in ch ...
Effect of cyclosporin A on prot ...
Denys–Drash syndrome (DDS) is characterized by progressive glomerulopathy caused by diffuse mesangial sclerosis (DMS), genitourinary defects, and a ...
Chronic pancreatitis in branche ...
A severe rare complication in patients with branched-chain organic acidurias (BCOA) is pancreatitis with a limited number of patients published so f ...