Hospital admission in children up to the age of 2 years.

abstract：:We report a 19-year-old boy with an interstitial deletion of the long arm of chromosome 8 (46, XY, del(8)(pter----q23.3: :q24.13----qter)). He shows the typical clinical symptoms of tricho-rhino-phalangeal syndrome (TRPI) and severe mental retardation, however without multiple exostoses. This is the second report of a...

journal_title：European journal of pediatrics

authors： Hamers A,Jongbloet P,Peeters G,Fryns JP,Geraedts J

更新日期：1990-06-01 00:00:00

abstract：:This was a retrospective study documenting all pacemaker implantations (PMIs) secondary to postoperative atrioventricular block. A total of 26 patients were included between 2011 and 2020. The incidence rate was 1.8%, with a median follow-up time of 4.5 years. At the time of the initial PMI, the median weight was 5 kg...

journal_title：European journal of pediatrics

authors： Ebrahim MA,Ashkanani HK,Alramzi RS,Malhas ZI,Al-Bahrani M,Sadek AA,Elsayed MA,Lyubomudrov VG

更新日期：2020-12-01 00:00:00

abstract：:An adolescent girl with severe thrombotic thrombocytopenic purpura (TTP) remained in a critical condition after 3 weeks of combined treatment with antiplatelet drugs, plasma infusions and plasma exchange. The introduction of vincristine resulted in gradual improvement and eventual complete remission which lasted for 2...

journal_title：European journal of pediatrics

authors： Van Gool S,Brock P,Van Laer P,Van Damme-Lombaerts R,Proesmans W,Casteels-Van Daele M

更新日期：1994-07-01 00:00:00

abstract：:There is evidence pointing to a decrease of the glomerular filtration rate (GFR) in a subgroup of nephrotic children, likely secondary to hypovolemia. The aim of this study is to validate the use of urinary potassium to the sum of potassium plus sodium ratio (UK/UK+UNa) as an indicator of hypovolemia in nephrotic synd...

journal_title：European journal of pediatrics

authors： Keenswijk W,Ilias MI,Raes A,Donckerwolcke R,Walle JV

更新日期：2018-01-01 00:00:00

abstract：:Spontaneous pneumomediastinum is uncommon in paediatric practice. We describe two cases of spontaneous pneumomediastinum in a child and an adolescent with anorexia nervosa. Thorough investigation failed to reveal any underlying cause for secondary pneumomediastinum. Pneumomediastinum in anorexia nervosa can be caused ...

journal_title：European journal of pediatrics

authors： van Veelen I,Hogeman PH,van Elburg A,Nielsen-Abbring FW,Heggelman BG,Mahieu HF

更新日期：2008-02-01 00:00:00

abstract：:Neonatal acute respiratory distress syndrome (NARDS) reflects pulmonary surfactant dysfunction, and the usage of bovine surfactant (Calsurf) supplement may therefore be beneficial. To determine whether bovine surfactant given in NARDS can improve oxygenation and survival rate, we conducted a multicenter, randomized tr...

journal_title：European journal of pediatrics

authors： Rong Z,Mo L,Pan R,Zhu X,Cheng H,Li M,Yan L,Lang Y,Zhu X,Chen L,Xia S,Han J,Chang L

更新日期：2020-10-21 00:00:00

abstract：:Kawasaki disease (KD) is associated with coronary artery injury. Studies have shown that the endothelial progenitor cell (EPC) participates in the process of arterial repair. Data have been reported that the number of EPC increased significantly in the subacute phase of KD. However, until now, there are no data about ...

journal_title：European journal of pediatrics

authors： Xu MG,Men LN,Zhao CY,Zhao X,Wang YX,Meng XC,Shen DR,Meng BY,Zhang Q,Wang T

更新日期：2010-03-01 00:00:00

abstract：UNLABELLED:Non-immune hydrops fetalis may find its origin within genetically determined lymphedema syndromes, caused by mutations in FOXC2 and SOX-18. We describe a newborn girl, diagnosed with non-immune hydrops fetalis at a gestational age of 30 weeks. Family history revealed the presence of an autosomal dominant lat...

journal_title：European journal of pediatrics

authors： de Bruyn G,Casaer A,Devolder K,Van Acker G,Logghe H,Devriendt K,Cornette L

更新日期：2012-03-01 00:00:00

abstract：:Co-trimoxazole is an effective antibacterial agent for the prophylaxis of urinary tract infection. Because experimental evidence raises the possibility that high-dose cotrimoxazole might interfere with normal somatic growth, the longitudinal growth and growth velocities were analysed in 114 girls receiving long-term, ...

journal_title：European journal of pediatrics

authors： Smellie JM,Preece MA,Paton AM

更新日期：1983-09-01 00:00:00

abstract：UNLABELLED:Mycobacterium bovis Bacillus Calmette-Guerin (BCG) is an attenuated live vaccine that may cause life-threatening clinical disease in children with impaired immunity. In particular, patients with any of the nine known inherited disorders of the interleukin-12/23 interferon-gamma (IL-12/23-IFNgamma) axis are h...

journal_title：European journal of pediatrics

authors： Ulrichs T,Fieschi C,Nevicka E,Hahn H,Brezina M,Kaufmann SH,Casanova JL,Frecerova K

更新日期：2005-03-01 00:00:00

abstract：:Cardiovascular abnormalities were evaluated in 64 children aged between 1 year 9 months and 25 years with mucopolysaccharidoses (MPS) and related disorders. A heart murmur was heard in 18 patients, but in only 6 was it characteristic for specific valvular lesions. Echocardiography was performed in 63 children. In one ...

journal_title：European journal of pediatrics

authors： Dangel JH

更新日期：1998-07-01 00:00:00

abstract：:A 2-month-old infant was admitted to hospital because of recurrent vomiting for 1 week, progressive apathy, and focal seizures. The cranial MRI showed a noticeable result. ...

journal_title：European journal of pediatrics

authors： Larsen A,Martin C,Meyer S,Rohrer T,Papanagiotou P,van der Knaap M,Gortner L

更新日期：2012-06-01 00:00:00

abstract：:A male infant with transient citrullinemia is described. Initially, he was found to have hypertyrosinemia and hypermethioninemia upon routine neonatal screening for inborn errors of metabolism performed at 4 days of age and was revealed to have citrullinemia upon detailed examination of plasma amino acids. At 30 days ...

journal_title：European journal of pediatrics

authors： Ohtake A,Takayanagi M,Ogura N,Nakajima H

更新日期：1983-10-01 00:00:00

abstract：:The results of 24 h oesophageal pH monitoring, performed in 129 infants aged 6-10 weeks, were compared to those in the same patients after shorter periods (3, 6, 9 and 12 h). In the investigated population there was no significant difference between the reflux index (percentage of time with a pH < 4.0) after 12 or 24 ...

journal_title：European journal of pediatrics

authors： Vandenplas Y,Casteels A,Naert M,Derde MP,Blecker U

更新日期：1994-02-01 00:00:00

abstract：UNLABELLED:It has been suggested that chronic treatment with L-thyroxine (L-T4) could be implicated in reducing bone mineral density (BMD). The purpose of this longitudinal study was to determine whether appendicular and axial BMD is decreased by L-T4 treatment in adolescent girls. Thirteen adolescent girls with subcli...

journal_title：European journal of pediatrics

authors： Saggese G,Bertelloni S,Baroncelli GI,Costa S,Ceccarelli C

更新日期：1996-06-01 00:00:00

abstract：UNLABELLED:Primary spontaneous pneumothorax (PSP) is not uncommon, and its recurrence is often a challenging clinical problem. Surgical management and predisposing factors for the recurrence of PSP, however, have not yet been well elucidated in adolescent patients. The major aim of this study was to investigate factors...

journal_title：European journal of pediatrics

authors： Chiu CY,Chen TP,Wang CJ,Tsai MH,Wong KS

更新日期：2014-11-01 00:00:00

abstract：:Regional variations in the human leucocyte antigen (HLA) distribution patterns of coeliac disease (CD) have been reported. This study focuses on phenotype frequencies of a cohort of Austrian paediatric CD patients in comparison with those recorded in the literature. HLA class I and II typing was performed in 136 CD pa...

journal_title：European journal of pediatrics

authors： Winklhofer-Roob BM,Rossipal E,Lanzer G

更新日期：1991-08-01 00:00:00

abstract：:Of 496 neonates and infants less than 1 year of age admitted to the paediatric surgical intensive care unit (PSICU) over a 5 year period (1983-1987), 94 required total parenteral nutrition (TPN) for more than 14 consecutive days, generally due to congenital anomalies of the digestive tract. Cholestasis occurred in 15 ...

journal_title：European journal of pediatrics

authors： Bos AP,Tibboel D,Hazebroek FW,Bergmeijer JH,van Kalsbeek EJ,Molenaar JC

更新日期：1990-02-01 00:00:00

abstract：:The United Nations Convention of Children's Rights (UNCRC) introduced in 1989 has generated a global movement for the protection of children's rights and has brought about a paradigm change in how children are perceived. Pediatric healthcare professionals are interacting with children and therefore with children's rig...

journal_title：European journal of pediatrics

authors： Streuli JC,Michel M,Vayena E

更新日期：2011-01-01 00:00:00

abstract：:We present a case of Pott's disease, where the patient presented with neurological impairment due to vertebral granulomatous necrosis, needing immediate decompression and later stabilizing and reconstructive orthopaedic surgery, in order to create awareness for TB in general, especially this forgotten form of spinal t...

journal_title：European journal of pediatrics

authors： van Well GT,van der Mark LB,Vermeulen RJ,van Royen BJ,Wuisman PI,van Furth AM

更新日期：2007-10-01 00:00:00

abstract：:We report a 13 year-old girl with manifestations strikingly reminiscent of the tricho-rhino-phalangeal (TRP) II or Langer-Giedion syndrome. A terminal deletion of 8q must be assumed to be the cause of her condition till proven otherwise. A similar chromosome abnormality should be searched for (blindly) in other cases ...

journal_title：European journal of pediatrics

authors： Bühler EM,Bühler UK,Stalder GR,Jani L,Jurik LP

更新日期：1980-03-01 00:00:00

abstract：:Positional plagiocephaly (PP) denotes flattening of the skull that occurs frequently in healthy infants. Aim of this study was to estimate the prevalence of positional plagiocephaly and to identify the risk factors in a cohort of healthy infants in order to help prevention of PP. In a prospective design, all healthy f...

journal_title：European journal of pediatrics

authors： Ballardini E,Sisti M,Basaglia N,Benedetto M,Baldan A,Borgna-Pignatti C,Garani G

更新日期：2018-10-01 00:00:00

abstract：UNLABELLED:Cleidocranial dysplasia (CCD; MIM 119600) is an autosomal dominant skeletal dysplasia characterised by hypoplastic clavicles, patent fontanelles, short stature, tooth anomalies and other variable skeletal changes. Different mutations of the RUNX2/CBFA1 gene (MIM 600211) have been detected in patients with CC...

journal_title：European journal of pediatrics

authors： Morava E,Kárteszi J,Weisenbach J,Caliebe A,Mundlos S,Méhes K

更新日期：2002-11-01 00:00:00

abstract：:Congenital adrenal hyperplasia (CAH) is an inherited metabolic disease caused by the deficiency of one of the enzymes necessary for cortisol synthesis. With carefully supervised medical treatment, CAH patients have the capacity for normal puberty and fertility. We report on a 12.4-year-old female who, because of the e...

journal_title：European journal of pediatrics

authors： Tahirovic H,Toromanovic A,Grubic M,Grubic Z,Dumic K

更新日期：2009-07-01 00:00:00

abstract：:Recent studies revealed that fluid overload is associated with higher mortality in critically ill children and adults. This study aimed to evaluate the association between fluid overload in the first 3 days of life and mortality in extremely low birth weight infants. This single-center retrospective cohort study inclu...

journal_title：European journal of pediatrics

authors： Matsushita FY,Krebs VLJ,Ferraro AA,de Carvalho WB

更新日期：2020-11-01 00:00:00

abstract：UNLABELLED:The inherited ion channel disorders (channelopathies) are a group of disorders caused by mutations in genes encoding ion channels. Ion channel disorders can affect any tissue, but the majority affect skeletal muscle or the central nervous system. These disorders include skeletal muscle sodium channelopathies...

journal_title：European journal of pediatrics

authors： Surtees R

更新日期：2000-12-01 00:00:00

abstract：:As simple and nonsurgical means of differentiating biliary atresia (BA) from intrahepatic cholestasis of unknown origin (IC), liver function tests including serum lipoprotein-X (LP-X) and gamma-glutamyltranspeptidase (GGTP) were done and evaluated for their usefulness in the diagnosis of 27 cholestatic Japanese young ...

journal_title：European journal of pediatrics

authors： Tazawa Y,Yamada M,Nakagawa M,Tada K,Konno T,Ohi R,Kasai M

更新日期：1986-04-01 00:00:00

abstract：UNLABELLED:The aim of this study was to obtain comprehensive data on clinical presentation, microbiology, computed tomography, surgical findings and histology in acute, sub-acute and chronic mastoiditis. We performed a prospective, observational study in children under 16 years of age presenting to our institution duri...

journal_title：European journal of pediatrics

authors： Stähelin-Massik J,Podvinec M,Jakscha J,Rüst ON,Greisser J,Moschopulos M,Gnehm HE

更新日期：2008-05-01 00:00:00

abstract：:Though children with Perlman and Wiedemann-Beckwith syndromes have a number of features in common, the two conditions are probably separate entities. The distinction may not always be easy, however, partly because of the extreme rarity of Perlman syndrome, only nine cases of which have been reported so far. We report ...

journal_title：European journal of pediatrics

authors： Grundy RG,Pritchard J,Baraitser M,Risdon A,Robards M

更新日期：1992-12-01 00:00:00

abstract：:An 11-year-old boy with chronic granulomatous disease caused by cytochrome b deficiency developed right upper lung lobe aspergillosis. Intracerebral lesions developed on maximum doses of flucytosine and amphotericin B. Treatment with 16 mg/kg oral itraconazole was followed by a dramatic clinical improvement and almost...

journal_title：European journal of pediatrics

authors： Kloss S,Schuster A,Schroten H,Lamprecht J,Wahn V

更新日期：1991-05-01 00:00:00